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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 10-K
|X| ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES
EXCHANGE ACT OF 1934
For the year ended December 31, 2003
OR
|_| TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES
EXCHANGE ACT OF 1934
Commission File No. 0-12991
LANGER, INC.
(Exact name of Registrant as specified in its charter)
Delaware 11-2239561
(State or other jurisdiction (I.R.S. employer
of incorporation or organization) identification number)
450 Commack Road, Deer Park, New York 11729-4510
(Address of principal executive offices) (Zip code)
Registrant's telephone number, including area code: (631) 667-1200
Securities registered pursuant to Section 12(b) of the Act: None
Securities registered pursuant to Section 12(g) of the Act:
Common Stock, par value $.02 per share
Title of Class
* * * * * * * * * * *
Indicate by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities Exchange Act of
1934 during the preceding 12 months (or for such shorter period that the
Registrant was required to file such reports), and (2) has been subject to such
filing requirements for the past 90 days.
YES |X| NO |_|
1
Indicate by check mark if disclosure of delinquent filers pursuant to Item 405
of Regulation S-K is not contained herein, and will not be contained, to the
best of registrant's knowledge, in definitive proxy or information statements
incorporated by reference in Part III of this Form 10-K or any amendment to this
Form 10-K. |X|
Indicate by check mark whether the registrant is an accelerated filer (as
defined in Rule 12b-2 of the Act):
YES |_| NO |X|
As of June 30, 2003 (i.e., the last day of Registrant's most recently completed
second quarter), the aggregate market value of voting stock held by
non-affiliates of the registrant was $4,812,586, as computed by reference to the
closing price of such common stock ($3.15) multiplied by the number of shares of
voting stock outstanding on June 30, 2003 held by non-affiliates (1,527,805
shares). Exclusion of shares from the calculation of aggregate market value does
not signify that a holder of any such shares is an "affiliate" of the Company.
Indicate the number of shares outstanding of each of the registrant's classes of
common stock as of March 24, 2004.
Class of Common Stock Outstanding at March 24, 2004
--------------------- -----------------------------
Common Stock, par value 4,447,451 shares
$.02 per share
DOCUMENTS INCORPORATED BY REFERENCE
The information required by Part III of this report is incorporated herein by
reference to the Company's proxy statement for the 2004 annual meeting of the
registrant's stockholders or amendment hereto which will be filed not later than
120 days after the end of the fiscal year covered by this report.
2
LANGER, INC.
FORM 10-K
TABLE OF CONTENTS
PAGE
PART I
ITEM 1. BUSINESS.......................................................... 8
ITEM 2. PROPERTIES........................................................ 16
ITEM 3. LEGAL PROCEEDINGS................................................. 16
ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS............... 16
PART II
ITEM 5. MARKET FOR REGISTRANT'S COMMON EQUITY AND RELATED
STOCKHOLDER MATTERS............................................... 17
ITEM 6. SELECTED FINANCIAL DATA........................................... 19
ITEM 7. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL
CONDITION AND RESULTS OF OPERATIONS............................... 20
ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT
MARKET RISK....................................................... 30
ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA....................... 31
ITEM 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON
ACCOUNTING AND DISCLOSURE......................................... 61
ITEM 9A. CONTROLS AND PROCEDURES........................................... 61
PART III
ITEM 10. DIRECTORS AND EXECUTIVE OFFICERS OF THE COMPANY................... 61
ITEM 11. EXECUTIVE COMPENSATION............................................ 61
ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS
AND MANAGEMENT.................................................... 61
ITEM 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS.................... 62
ITEM 14. PRINCIPAL ACCOUNTANT FEES AND SERVICES............................ 62
PART IV
ITEM 15. EXHIBITS, FINANCIAL STATEMENTS, FINANCIAL STATEMENT
SCHEDULES, AND REPORTS ON FORM 8-K................................ 63
SIGNATURES.................................................................. 67
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PART I
Factors that May Affect Future Results and Investment in the Company
In addition to other information in this Annual Report on the Form 10-K, the
following risk factors should be carefully considered in evaluating our business
because such factors may have a significant impact on our business, operating
results, liquidity and financial condition. As a result of the risk factors set
forth below, actual results could differ materially from those projected in any
forward-looking statements. Additional risks and uncertainties not presently
known to us, or that we currently consider to be immaterial, may also impact our
business, operating results, liquidity and financial condition. If any of the
following risks occur, our business, operating results, liquidity and financial
condition could be materially adversely affected.
We have a history of net losses and may incur additional losses in the future.
We have a history of net losses. In order for us to achieve and maintain
consistent profitability from our operations, we must continue to achieve
product revenue at or above current levels. We may increase our operating
expenses as we attempt to expand our product line and acquire other businesses
and products. As a result, we will need to increase our revenues significantly
to achieve sustainable profitability. We cannot assure you that we will be able
to obtain sustainable profitability. Any such failure could have a material
adverse effect on our business, financial condition, and results of operations.
A significant portion of our revenues is derived from custom orthotic devices,
and our future success may depend on the continued acceptance and growth of
these products.
For the year ended December 31, 2003, approximately 77% of our sales were
derived from custom orthotic devices. Any material adverse developments with
respect to the market acceptance, sale or use of our custom orthotic devices
could, therefore, significantly affect our revenues and have a material adverse
effect on our business, financial condition and results of operations. The level
of market acceptance of our custom orthotic devices could be affected by a
number of factors, including:
o the effectiveness of our sales and marketing efforts;
o unfavorable publicity regarding our products;
o the price and performance of our products relative to competing
products; and
o changes in government and third-party pay or reimbursement policies
and practices with respect to custom orthotic devices.
If we fail to execute our growth strategy, we may not become profitable or
achieve sustainable profitability.
A key element of our growth strategy is the acquisition of businesses and assets
that will complement our current businesses, increase our size, expand our
geographic scope of operations, and otherwise offer growth opportunities. We may
not be able to successfully identify attractive acquisition opportunities,
obtain financing for acquisitions or satisfactory terms or successfully acquire
identified targets. Additionally, competition for acquisition opportunities in
our industry may escalate, thereby increasing the costs to us of completing
acquisitions or cause us to refrain
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from making acquisitions. Our growth strategy also depends on our ability to
hire and train new staff and managerial personnel, and adapt our structure to
comply with present or future legal requirements affecting our arrangements with
our healthcare professional customer base. Our ability to implement our growth
strategy is also subject to other risks and costs, including;
o difficulties in assimilating acquired operations or products;
o the risk of losing key employees, customers or suppliers of acquired
businesses;
o diversion of management's attention from our core business;
o adverse effects on existing business relationships with suppliers
and customers;
o our ability to realize operating efficiencies, synergies, or other
benefits expected from an acquisition;
o risk associated with entering markets in which we have limited or no
experience; and
o assumption of contingent liabilities of acquisition targets.
Our failure to successfully implement our growth strategy could have a material
adverse effect on our business, financial condition and results of operations.
We may not be able to adequately manage our rapid growth.
We have rapidly expanded, and are seeking to continue to rapidly expand, our
business. This growth has placed significant demands on management,
administrative, operating and financial resources. The continued growth of our
customer base, the types of products offered and geographic markets served can
be expected to continue to place a significant strain on our resources.
Personnel qualified both in the production of our products and the marketing of
such products are difficult to find and hire and enhancement of management
systems to support growth are difficult to implement. Our future performance and
profitability will depend in large part on our ability to attract and retain
additional management and other key personnel, ability to implement successful
enhancements to management systems and our ability to adapt those systems, as
necessary, to respond to growth in our business. No assurance can be made that
we will be able to successfully achieve our objectives. Any such failure could
have a material adverse effect on our business, financial condition, and results
of operations.
We may face difficulties integrating the operations of acquired businesses.
Part of our growth strategy has been and will continue to be the acquisition of
businesses. Our ability to integrate the operations of these businesses is
subject to various risks, and we may not be able to realize the operating
efficiencies, synergies, or other benefits expected from these acquisitions. Our
failure to successfully integrate the operations of these acquired businesses in
a timely manner without incurring unexpected costs could have a material adverse
effect on our business, financial condition, and results of operations.
We may not be able to raise adequate financing to fund our operations and growth
prospects.
Our acquisition and product expansion programs, debt servicing requirements, and
existing operations may require substantial capital resources. We cannot assure
you that we will be able to generate sufficient operating cash flow or obtain
sufficient additional financing to meet these requirements. Failure to achieve
our financing objectives could require us to reduce operating costs by altering
and delaying our business plan or otherwise radically altering our business
practices. Such failure could have a material adverse effect on our business,
financial condition, and results of operations.
Our existing purchasing arrangements may be adversely affected if we are unable
to maintain good relations with our suppliers.
We currently enjoy favorable terms with most of our suppliers, including the
third party manufacturer of PPT(R), a primary fabrication material used in many
of our products. Our ability to sustain gross margins has been, and will
continue to be, dependent, in part, on our ability to maintain such terms. These
terms may be adversely impacted by changes in our suppliers' strategies or
changes in relationship with suppliers. Our inability to maintain such
5
terms or the inability of the third party to manufacture and deliver to us
sufficient quantities of PPT(R) , could have a material adverse effect on our
business, financial condition and results of operations.
If we fail to cultivate new or maintain established relationships with medical
professional customers, our revenue may decline.
Our success is, in large part, dependent upon the referrals and recommendations
of licensed healthcare professionals and therapists and our ability to market
products to them. Healthcare professionals and therapists who recommend our
products are not our employees and are free to recommend competitors' products.
If we are unable to successfully cultivate and maintain relationships with, and
market our products to, these healthcare professionals and therapists, we may
receive fewer orders for products and revenues may decline, which could have a
material adverse effect on our business, financial condition, and results of
operations.
The nature of our business could subject us to potential product liability and
other claims.
The sale of orthotic products and other biomechanical devices entails the
potential risk of physical injury to patients and an inherent risk of product
liability and other similar claims. We believe that we maintain adequate
insurance coverage for our products. However, we cannot assure you that this
coverage would be sufficient to cover the payment of any potential claim. In
addition, we cannot assure you that this or any other insurance coverage will
continue to be available or, if available, will be obtainable at a reasonable
cost. A partially or completely uninsured material loss could have a material
adverse effect on our business, financial condition and results of operations.
Health care regulations or health care reform initiatives could materially
adversely affect our business, financial condition and results of operations.
We are subject to governmental regulation and supervision both in the United
States, at the federal and state level, and abroad, including anti-kickback
statures, self-referral laws, and fee-splitting laws. In some cases, we may be
required to obtain regulatory approvals and otherwise comply with regulations
regarding safety, quality and efficacy standards. Our failure to obtain such
approvals or comply with applicable regulatory requirements could result in
government authorities taking punitive actions against us, including, among
other things imposing fines and penalties or preventing us from manufacturing or
selling products. We cannot assure you that these laws and regulations will not
change or be interpreted in the future in a manner which restricts or adversely
affects our business activities or relationships with providers of orthotic and
orthopedic products.
Changes in government and other third party payor or reimbursement levels could
adversely affect our revenues and profitability.
We derived a portion of our revenues from sales programs to parties reimbursed
by Medicare, workers compensation insurance, or other insurers. Many of these
programs set maximum reimbursement levels for orthotic products. We may be
unable to sell our products on a profitable basis if third-party payors deny
coverage or reduce their current levels of reimbursement. The percentage of our
sales dependent on Medicare or other insurance programs may increase as the
portion of the U.S. population over age 65 continues to grow, making us more
vulnerable to reimbursement level reductions by these organizations. Reduced
government reimbursement levels could result in reduced private payor
reimbursement levels because of indexing of Medicare fee schedules by certain
third-party payors. (Furthermore, the healthcare industry is experiencing a
trend towards cost containment.) This trend could adversely affect net sales and
could have a material adverse effect on our business, financial condition, and
results of operations.
Our business is highly competitive.
Our business is highly competitive in all product lines. Certain of our
competitors may have more depth and experience of personnel as well as more
recognizable trademarks for products similar to those sold by us. In addition,
our competitors may develop or improve their products, in which event our
products may be rendered
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obsolete or less marketable. We expect that the level of competition may
increase in the future. There can be no assurance that we will be able to
continue to compete successfully. Any such failure could have a material adverse
effect on our business, financial condition, and results of operations.
New therapeutic techniques or products could decrease the demand for our
products.
The medical industry is consistently searching for improved techniques and
products to improve patient care and treatment. New surgical techniques,
therapeutic procedures, and alternative products could cause healthcare
professionals to decrease orders for our custom orthotic products. Such a
decrease would have a material adverse impact on our business, financial
condition and results of operations.
Loss of the services of key management personnel could adversely affect our
business.
Our operations are dependent upon certain key management personnel, including
our President and Chief Executive Officer. The unexpected loss of the services
of such key management personnel could have a material adverse effect on our
business, financial condition, and results of operations.
We may be unable to protect our proprietary technology.
We are dependent upon a variety of methods and techniques that we regard as
proprietary trade secrets. We are also dependent upon a variety of trademarks,
service marks and designs to promote brand name development and recognition. We
rely on a combination of trade secrets, copyright, patent, trademark, unfair
competition and other intellectual property. Due to the difficulty of monitoring
unauthorized use of and access to intellectual property, however, such measures
may not provide adequate protection. In addition, there can be no assurance that
courts will always uphold our intellectual property rights, or enforce the
contractual arrangements that we have entered into to protect our proprietary
technology. Any unenforceability or misappropriation of our intellectual
property could have a material adverse effect on our business, financial
condition and results of operations. In addition, if we bring or become subject
to litigation to defend against claimed infringement of our rights or of the
rights of others or to determine the scope and validity of our intellectual
property rights, such litigation could result in substantial costs and diversion
of our resources which could have a material adverse effect on our business,
financial condition and results of operations. Unfavorable results in such
litigation could also result in the loss or compromise of our proprietary
rights, subject us to significant liabilities, require us to seek licenses from
third parties, or prevent us from selling our products, which could have a
material adverse effect on our business, financial condition and results of
operations.
A portion of our revenues and expenditures is subject to exchange rate
fluctuations that could adversely affect our reported results of operations.
While a majority of our business in denominated in the United States dollars, we
maintain operations in foreign countries, primarily the United Kingdom and
Canada, that require payments in the local currency and payments received from
customers for goods sold in these countries are typically in the local currency.
Consequently, fluctuations in the rate of exchange between the U.S. dollar and
certain other local currencies may affect our results of operation and
period-to-period comparison of our operating results.
One stockholder has the ability to significantly influence the election of our
directors and the outcome of corporate action requiring stockholder approval.
As of March 23, 2004 Warren B. Kanders, in his capacity as sole manager and
voting member of Langer Partners, LLC and the sole shareholder of Kanders &
Company, Inc., may be deemed to be the beneficial owner of 2,008,523 shares of
our common stock or approximately 40.5% of our common stock. In addition, our
officers and directors beneficially own an aggregate of 1,810,927 shares of our
common stock, or approximately 37%, of our common stock. Consequently, Mr.
Kanders together with our officers and directors will have the ability to
significantly influence the election of our directors and the outcome of
corporate actions requiring stockholder approval, including a change in control.
7
The price of our common stock may be volatile, which could effect a
stockholder's return on investment.
The market price of our common stock has been subject to a significant
fluctuations, and we expect it to continue to be subject to such fluctuations
for the foreseeable future. We believe the reasons for these fluctuations
include the relatively thin level of trading in our stock, and the relatively
low public float. Therefore, variations in financial results, announcements of
material events by us or our competitors, our quarterly operating results,
changes in general conditions in the economy or the health care industry, other
developments affecting us or our competitors or general price and volume
fluctuation in the market could cause the market price of the common stock to
fluctuate substantially.
We have a significant amount of convertible indebtedness outstanding and may
issue a substantial amount of our common stock in connection with future
acquisitions and growth plans and the sale of those shares could adversely
affect our stock price.
On October 31, 2001, we sold $14,589,000 of convertible subordinated notes in a
private placement. The notes are convertible into approximately 2,431,500 shares
of our common stock, subject to adjustment in certain circumstances. In
connection with acquisitions we completed in 2002 and 2003, we issued, in the
aggregate, 169,416 shares of common stock. We anticipate that we would issue
additional shares of our common stock and may also issue additional convertible
debt to finance possible future acquisitions. The number of outstanding shares
of our common stock that will be eligible for sale in the future is, therefore,
likely to increase substantially. Persons receiving shares of our common stock
in connection with these acquisitions or financings may be more likely to sell
large quantities of their common stock, which may impact the price of our common
stock. In addition, the potential issuance of additional shares in connection
with anticipated acquisitions could lessen demand for our common stock and
result in lower price than would otherwise be obtained. Additional shares sold
to finance acquisitions and conversions of convertible indebtedness may also
dilute our earnings per share.
Issuance by us of authorized preferred stock can have adverse effects, including
dilution and discouragement of takeovers.
Our certificate of incorporation contains certain provisions that may delay or
prevent a takeover. Our Board of Directors has the authority to issue up to
250,000 shares of preferred stock, and to determine the price, rights,
preferences, and restrictions, including voting and conversion rights, of those
shares without nay further action or vote by the stockholders. The rights of the
holders of common stock will be subject to, and may be adversely affected by,
the rights of the holders of preferred stock that my be issued in the future.
Such provisions could adversely affect the holders of commons stock in a variety
of ways, including by potentially discouraging, delaying or preventing a
takeover of the Company and by diluting our earnings per share.
We do not intend to pay dividends.
We currently do not intend to pay any dividends on our common stock. We
currently intend to retain any earnings for working capital, repayment of
indebtedness, capital expenditures and general corporate purposes.
ITEM 1. BUSINESS
Langer, Inc. (the "Company or "we") is a leading orthotics products company
specializing in designing, manufacturing, distributing and marketing high
quality foot and gait-related biomechanical products. The Company's diversified
range of products is comprised of (i) custom orthotic devices ordered by
healthcare professionals and (ii) pre-fabricated orthopedic rehabilitation and
recovery devices distributed by the Company to healthcare professionals. Since
January 1, 2002, the Company has operated in two segments, custom orthotics and
distributed products.
8
Custom Orthotics
The Company's custom orthotic devices are contoured molds, purchased by a
healthcare professional for a patient, which are worn in the shoe to correct
biomechanical foot and postural disorders in patients which often result in pain
or discomfort, or otherwise impede an individual's ability to maintain a normal
gait. The Company also provides custom devices which support or control the
ankle region (ankle foot orthosis).
Distributed Products
The Company's distributed products are manufactured by others and consist of;
(i) prefabricated products for the lower extremities and (ii) a selection of
therapeutic footware. These products, which supplement our custom orthotic
product line, consist of modular shoe inserts, ankle braces, compression hose,
socks, and therapeutic shoes and sneakers, and are purchased by healthcare
professionals for use by their patients. In addition, we distribute PPT(R) to
manufacturers who incorporate PPT(R) into their products. PPT(R) is a soft
tissue cushioning material made from medical grade urethane produced in
laminated sheet form, molded insoles, and components for orthotic devices.
Industry Background
The Company competes in the portion of the orthopedic rehabilitation and
recovery market segment which manufactures, markets, sells, and distributes
orthopedic products and retail orthopedic products. The Company estimates that
global orthopedic rehabilitation and recovery market revenues exceed $8 billion
annually. The Company believes the estimated revenues of the orthopedic products
markets in which we compete exceed $2 billion annually.
The Company believes the growth of these markets is being driven by strong
demographic and other trends, including:
o an aging population who historically have required a higher than
average percentage of orthotic and orthopedic products and services
than the general population;
o a growth rate of persons 65 and older which is nearly triple that of
the balance of the population;
o an increased participation in exercise, sports, and other physical
activities by all age groups which has directly led to increased
orthopedic related strains and injuries requiring orthotic and
related products;
o a growing awareness of the importance of prevention and
rehabilitation of orthopedic injuries; and
o an industry-wide consolidation leading to greater marketing and
sales resources.
Podiatrists in the United States are the largest single source for the purchase
of custom foot orthotic products. In the United States, Medicare and most other
health care organizations that provide coverage for foot orthotics require a
podiatrist or other licensed doctor to write a prescription and indicate the
diagnosis and need for the custom orthotic. Due to the nature of this
reimbursement environment, little effort is directed at marketing to the end
user of the product. Instead, custom orthotics manufacturers market and
distribute their foot orthotic laboratory services to healthcare professionals,
including podiatrists, chiropractors, orthopedic surgeons,
orthotists/prosthetists, physical therapists, and athletic trainers.
While the market for custom orthotics outside the United States is similar in
size to the United States market, prefabricated orthotic devices are generally
preferred in Europe due to reimbursement policies. The Company currently markets
its products in Canada and the United Kingdom, markets where favorable national
reimbursement and payment structures prevail. The Company also markets its
products in thirty other countries.
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Growth Strategy
The Company expects the demand for orthotic products will continue to grow. We
plan to execute our growth strategy primarily through internal expansion by
offering additional products through our marketing channels and through
strategic acquisitions of businesses offering complementary services, markets,
and customer bases. In January 2003 the Company completed the acquisition of
Bi-Op Laboratories, Inc.("Bi-Op"). The acquisition provides the Company with a
complementary market, a synergistic business model and potential manufacturing
efficiencies. The following elements define our growth strategy:
Pursue Strategic Acquisitions. The foot orthotic products industry is highly
fragmented and characterized primarily by smaller, geographically restricted
manufacturers. As a result, we selectively pursue acquisitions that complement
and expand our product offerings and provide access to new geographic markets
and new medical practitioner relationships.
Expand Distribution Network and Product Offerings. The Company believes that a
broader product line will encourage additional healthcare professionals to order
custom orthotics products and will enhance our brand appeal with healthcare
professionals. We will seek to continue to expand our range of products through
the acquisition of niche product manufacturers and by investing in the
development of new and enhanced products which complement our existing offerings
and educational programs.
Broaden Product Offerings to Healthcare professional and Customer Base. The
Company will seek to increase penetration of our existing healthcare
professional and customer base with sales of additional products. We also intend
to increase customer satisfaction and strengthen our customer relationships
through expanded product offerings.
Research and Development. Lastly, the Company will continue where applicable to
conduct research and development to conceive and evaluate new or alternative
orthotics products and services. We believe that increased investment in
research and development can provide bases for new products and improved
practice management programs such as new techniques to measure and cast our
custom orthotics products. The Company did not make any expenditures in research
and development in 2003 and spent $164,872 and $142,192 on research and
development in 2002 and 2001, respectively. We expect to incur research and
development expenses in 2004.
Acquisitions
General
With continued advances in technology, the Company believes that the larger
orthotics manufacturers that employ advanced technologies will lower per unit
manufacturing costs, improve quality, accelerate turnaround time and will
continue to grow their overall share of the market. Concurrently, many of the
smaller orthotics manufacturers will find it increasingly difficult to remain
competitive and may not be able to access the capital required to purchase and
implement the required technological advances. Moreover, the Company believes
that many healthcare professionals in the industry would prefer to deal with a
consolidated entity that can provide a broad spectrum of branded orthotics
products. We believe that the orthopedic rehabilitation and recovery market will
consolidate as the smaller manufacturers are acquired by the larger, and faster
growing, manufacturers.
10
The Company expects to pursue a strategy of growth through acquisitions by
focusing on acquisitions of companies which have a core customer base similar to
ours and manufacture or sell products which are synergistic with our product
offerings. Orthotic manufacturing companies we may acquire are intended to
become hubs for further penetration into their industry niche or geographic
sales area. Generally, we will seek to streamline operations in acquired
companies to improve turnaround time and reduce expenses, resulting in economies
of scale, reduced general and administrative expenses and facilities
consolidation. We will seek to consolidate operations with our acquired product
manufacturing companies. This is intended to allow us to leverage efficiencies
and operational best practices.
The Company uses several criteria to evaluate prospective acquisitions,
including whether the business to be acquired:
o broadens the scope of the services or products we offer or the
geographic areas we serve;
o offers attractive margins;
o provides earnings accretion;
o offers the opportunity to enhance profitability by improving the
efficiency of our operations;
o offers consistent management with our existing businesses;
o complements our portfolio of existing businesses by increasing our
ability to manage our customers needs; and
o has a strong management team that is interested in continuing in
their roles with us.
Recent Acquisitions
On May 6, 2002, the Company acquired the net assets of Benefoot, Inc., and
Benefoot Professional Products, Inc. Benefoot, Inc., designs, manufactures and
distributes foot and gait-related biomechanical products, including custom-made
prescription orthotic devices, custom-made Birkenstock(R) sandals and
off-the-shelf orthotic devices to healthcare professionals. Benefoot
Professional Products markets and distributes footwear products to podiatrists.
The purchase price was $6.1 million of which $3.8 million was paid in cash, $1.8
million was paid through the issuance of promissory notes and $.5 million was
paid by issuing to the sellers 61,805 shares of the Company's common stock. The
Company also assumed certain liabilities including approximately $.3 million of
long term indebtedness. The Company also agreed to pay Benefoot up to an
additional $1.0 million upon satisfaction of certain performance targets from
May 6, 2002 to May 6, 2004. Through December 31, 2003, the Company had paid or
accrued $.6 million with respect to such obligation.
In January 2003, the Company acquired all the capital stock of Bi-Op
Laboratories, Inc. which is engaged in the development, manufacture and sale of
footwear products and foot orthotic devices. When converted to U.S. dollars the
total purchase price approximated $2.2 million of which $1.8 million (including
transaction costs) was paid in cash and $.4 million was paid by issuing 107,611
shares of the Company's common stock. The purchase price was funded by using a
portion of the proceeds remaining from the sale of the Company's 4% Convertible
Subordinated notes due August 31, 2006.
Products
The Company manufactures, markets, sells, and distributes two principal
categories of products: (i) custom orthotic devices ordered by healthcare
professionals and (ii) pre-fabricated orthopedic rehabilitation and recovery
devices and related devices sold to a patient by healthcare professionals. These
products are designed to provide relief from symptoms and complications arising
from (i) ankle, knee, pelvis, hip, and spinal pain caused by injuries and
biomechanical misalignment, (ii) diabetes, stroke, nerve damage, cerebral palsy,
multiple sclerosis and similar ailments, and (iii) post-operative recovery.
11
Custom Orthotic Devices
Orthotic foot devices, or foot orthoses, are contoured molds made from plastic,
graphite, or composite materials, depending upon the requirements of the
patient, which are placed in the patient's shoe to correct or mitigate
abnormalities in gait and relieve symptoms associated with foot or postural
misalignment. Orthotic devices help provide more normal function by maintaining
the angular anatomical relationships between the patient's forefoot, rearfoot,
leg and horizontal walking surface. Accordingly, muscle is enhanced and the
efficiency and smoothness of weight stress transmission through the feet and
legs are improved. The result is a reduction of abnormal motion without total
restriction of normal motion and an increase in foot and leg stability. Foot
problems may be alleviated or eliminated, as well as leg and back fatigue caused
by improper muscle use.
Typically, when a healthcare professional orders a custom foot orthotic from the
Company, the healthcare professional will take a plaster cast or an imprint of
the patient's foot by having the patient stand on a piece of foam slightly
larger than the patient's foot. The plaster or foam cast is sent to our
laboratory where it is used to make a plaster cast or digitized scan of the
patient's foot, from which we manufacture and customize the orthotic insert. We
have implemented technology which permits a podiatrist to take measurements of a
patient's foot at several specified locations or make a scan of the patients
feet and transmit the measurements to us electronically. From these measurements
or scans, we make the model of the patient's foot, from which we manufacture and
customize the orthotic insert. This technology, along with CAD/CAM technology
and laser scanning, will enable us to reduce the time required and costs
associated with the production of our custom foot orthotics.
The Company also offers a full line of custom Ankle-Foot Orthoses (AFO's)
devices, which are used to support, align, prevent, correct, substitute or
enhance function, and decrease pain or discomfort of the foot and ankle. These
products are often used for the more difficult and challenging foot and ankle
injuries.
The Company's custom orthotic product offerings include:
o Sporthotics(R), designed for the specific needs of runners and other
sport-specific athletes, including football, basketball and tennis
players;
o Healthflex(R), designed for patients that participate in aerobic
exercise, high-power walking, or step classes;
o Design-Line(R), a functional orthotic designed to fit into dress
shoes, such as loafers and high fashion shoes, which cannot
accommodate a full-size orthotic; and;
o Slimthotics(R), a device for use in women's high-heeled shoes,
narrow flats, ballet slippers, tap shoes, and women's ballroom
dancing shoes.
Distributed Products
The Company distributes prefabricated orthotic devices and related orthotic
supplies and materials.
One of our lines of prefabricated foot orthotic products provides patients a low
cost alternative to a custom orthotic. We provide these products to a podiatrist
or other healthcare professional based upon several criteria, including shoe
size, and the healthcare professional sells the product to a patient based upon
the patient's needs.
In 2000, we launched our prefabricated foot orthoses, called Contours(TM), which
require no special casting by the healthcare professional. This off-the-shelf
product line, sold to healthcare professionals has been expanded to include
dress (low profile), sport and standard models and provides a lower cost option
when pricing is an issue.
12
The Company also provides orthopedic devices that are used in the treatment of
ailments of the lower leg. These include products which support or control the
ankle region (ankle foot orthoses). In addition, we market products that address
the diabetic market, including insoles, and a selection of footwear (shoes,
socks, and other related products) which offers protection for patients with
diabetes. We believe these ancillary product lines will help us achieve our goal
of being able to provide a variety of orthopedic needs for our core lower
extremity customer.
In many of our orthotic products, we use PPT(R), a medical grade soft tissue
cushioning material with a high density, open-celled urethane foam structure.
The essential function of PPT(R), which independent tests show to have improved
properties over competitive materials, is to provide protection against forces
of pressure, shock and shear. We believe that PPT's(R) characteristics make it a
superior product in its field. PPT(R) has a superior "memory" that enables it to
return to its original shape faster and more accurately than other materials
used for similar purposes. PPT(R) is also odorless and non-sensitizing to the
skin and has a porosity that helps the skin to remain dry, cool and comfortable.
These factors are especially important in sports medicine applications.
We have developed and sell a variety of products fabricated from PPT(R),
including molded insoles, components for orthotic devices and laminated sheets.
Some manufacturing operations associated with these products are performed by
outside vendors.
Besides podiatric use, we believe PPT(R) is suitable for other orthopedic and
medical-related uses such as liners for braces and prosthetics, as shock
absorbers and generally in devices used in sports and physical therapy. We
expect to expand our products to include shock absorbing PPT(R) slow recovery
material which will be produced as sheets to be sold to other manufacturers and
distributors, and as flat and contoured shoe inserts to be sold to healthcare
professionals.
Customers
The majority of the Company's sales are within the United States to podiatrists,
orthopedic surgeons, orthotists, physical therapists, and other health care
professionals. However, we also sell our products in the United Kingdom, Canada,
and 30 other countries. We intend to expand our product offerings into new
territories.
The Company markets its custom orthotic products primarily to podiatrists who
order the custom orthotic devices for their patients. However, we will seek to
broaden our referral channels by increased penetration of orthopedic surgeons,
physical therapists, orthotists, chiropractors, athletic trainers, and other
podiatrists currently working in the United States. We also anticipate that we
will seek to increase our referral channels outside the United States.
The Company sells its distributed products primarily to wholesale distributors
and healthcare professionals for sale to patients. For both our custom orthotics
and distributed products, healthcare professionals usually include the cost of
the orthotic products in the fee charged to the patient.
Marketing and Distribution
We believe that we have built strong name recognition and an excellent
reputation in the orthotics industry. We are seeking to become a more
comprehensive source of orthopedic supplies for health care professionals who
treat the lower extremities.
The Company utilizes a network of regional sales representatives to target
multi-practitioner and individual facilities. In addition, we use trade shows,
advertising, direct mail, educational sponsorships, public relations and
customer visits to market and distribute our products. We emphasize customer
service by maintaining a staff of customer service representatives.
13
The Company provides education and training for healthcare professionals who
treat biomechanical problems of the lower extremity through seminars and
in-service programs. We offer healthcare professionals a comprehensive program
in biomechanics, gait analysis and the cost-effectiveness of orthotic therapy.
The Company promotes awareness of orthotics through marketing and operational
initiatives. We maintain a volume incentive program and offer practice building
assistance to help healthcare professionals expand the orthotic components
portion of their practices. We believe these medical practitioner assistance
programs strengthen our relationships with our existing customer base.
Manufacturing and Raw Materials
The Company manufactures its custom orthotics and warehouses its distributed
products internally at its production facilities located in Deer Park, New York;
Brea, California; Montreal, Canada; and Stoke-on-Trent, England. We obtain most
of our fabrication materials other than PPT(R) from a variety of sources. We
believe that we maintain good relationships with these suppliers. However, if
necessary, we believe we could readily obtain alternate suppliers at a
competitive price. We are aware of multiple suppliers for these materials and
would not anticipate a significant impact if we were to lose any suppliers, and
we have not experienced any significant shortages other than occasional
backorders. To date, we have found that the components, supplies and raw
materials that are necessary for the manufacture, production and delivery of our
products have been available in the quantities that are required. However, the
failure of our suppliers to deliver components, supplies, and raw materials in
sufficient quantities and in a timely manner, and the inability to find
replacement suppliers, could adversely affect our business and results of
operations.
Competition
The market for orthotic products is highly competitive, and we compete with a
variety of companies ranging from small businesses to large corporations. The
Company believes the foot orthotics market is highly fragmented and regional
(and in many instances local) in nature. Although a few licensed medical
practitioners produce foot orthotics in-house, the custom orthotic market is
serviced primarily by third-party laboratories similar to the Company. Included
among these laboratories that sell nationally in the United States are Bergmann
Orthotic Laboratory, Foot Levelers, Inc., Footmaxx Holdings Inc., KLM Orthotic
Laboratories, Allied OSI Labs, ProLab Orthotics, and PAL Health Systems. We
estimate that, including Langer, these firms comprise approximately 35% of the
$250 million custom foot orthotics market in the United States.
The market for soft tissue products such as PPT(R) is highly competitive and
includes the following brand name products: Spenco, Sorbothane, and Poron.
In both the custom and distribution products markets, the principal competitive
factors are efficiencies of scale, quality of engineering and design, brand
recognition, reputation in the industry, production capability and capacity, and
price and customer relations. In the custom orthotic market, ability to meet
delivery schedules is another principal competitive factor. We believe that we
provide superior design and production expertise.
Medical Consultants
The Company has relationships with four medical specialists who provide
professional consultative services to the Company in their areas of
specialization. The consultants test and evaluate the Company's products, act as
speakers for the Company at symposiums and professional meetings, generally
participate in the development of the Company's products and services and
disseminate information about them. The Company also relies on practitioners in
various parts of the country to act as field evaluators of the Company's
products.
14
Employees
As of January 1, 2004, the Company had 247 employees, of which 144 were located
in Deer Park, New York, 33 were located in Brea, California, 33 were located in
Montreal, Canada and 33 were located in Stoke-on-Trent, England and four outside
salesmen. None of our employees are represented by unions or covered by any
collective bargaining agreements. The Company has not experienced any work
stoppages or employee-related slowdowns and believes that its relationship with
employees is satisfactory.
Patents and Trademarks
The Company holds a variety of patents, trademarks, and copyrights in several
countries, including the United States. We have exclusive licenses to three
types of orthotic devices which are patented in the United States and several
foreign countries. We believe that none of our active patents, trademarks, or
licenses are essential to the successful operation of our business as a whole.
However, one or more of the patents, trademarks, or licenses may be material in
relation to individual products or product lines. Loss of patent protection
could have an adverse effect on our business by permitting competitors to
utilize techniques developed by us.
Government Regulation
The jurisdictions in which we seek to market our products may regulate and
supervise our products and operations. In some circumstances, we may be required
to obtain regulatory approvals and otherwise comply with regulations regarding
safety, quality and efficacy standards. These regulations vary from country to
country, and the regulatory review can be lengthy, expensive and uncertain. In
the United States, we are subject to federal and state governmental regulation
and supervision, including anti-kickback statutes, self-referral laws, and
fee-splitting laws.
Seasonality
Revenue derived from the Company's sales of orthotic devices, a substantial
portion of the Company's operations, has in North America historically been
significantly higher in the warmer months of the year, while sales of orthotic
devices by the Company's United Kingdom subsidiary has historically not
evidenced any seasonality.
Where You Can Find More Information
Our Internet address is www.langerinc.com. We will make available free of charge
on or through our Internet website our annual report on Form 10-K, quarterly
reports on Form 10-Q, current reports on Form 8-K, and amendments to those
reports filed as soon as reasonably practicable after such material was
electronically filed with, or furnished to, the Securities and Exchange
Commission. The Company will also provide to any person without charge, upon
request, a copy of its Code of Business Conduct & Ethics. The Company intends to
disclose future amendments to the provisions of the Code of Business Conduct &
Ethics and waivers from the Code of Business Conduct & Ethics, if any, made with
respect to any our directors and executive officers, on its Internet site and/or
through the filing of a Current Report on Form 8-K with the Securities and
Exchange Commission. Materials the Company files with the Securities and
Exchange Commission may be read and copied at the Securities and Exchange
Commission's Public Reference Room at 450 Fifth Street, NW, Washington, D.C.
20549. This information may also be obtained by calling the Securities and
Exchange Commission at 1-800-SEC-0330. The Securities and Exchange Commission
also maintains an internet website that contains reports, proxy and information
statements, and other information regarding issuers that file electronically
with the Securities and Exchange Commission at www.sec.gov. The Company will
provide a copy of any of the foregoing documents to stockholders upon request.
Any such requests should be made in writing to the Company's Chief Financial
Officer, Joseph Ciavarella at 450 Commack Road, Deer Park, NY 11729-4510.
15
ITEM 2. PROPERTIES
We have manufacturing, warehouse, and office space at the following locations:
2004 Annual Owned/ Approximate
Location Rent(1) Leased Size
------------------------- ----------- --------- ---------------
Deer Park, NY $322,633 Leased(2) 44,500 sq. ft.
Deer Park, NY $ 14,700 Leased(3) 3,500 sq. ft.
Brea, CA $103,500 Leased(4) 9,300 sq. ft.
Stoke-on-Trent, England $ 23,343(5) Leased(5) 15,000 sq. ft.
Montreal, Canada -- Owned 7,800 sq. ft.
(1) 2004 annual rent is based upon firm leases in place at March 15,
2004.
(2) Principal executive office location. Expires at the end of July,
2005. We have the option to extend the lease for an additional four
(4) years.
(3) Expires on July 31, 2004. This lease will be terminated as certain
warehouse facilities have been consolidated.
(4) Expires on December 31, 2004.
(5) Based upon an exchange rate of $1.7785 dollars per British pound.
The lease is scheduled to expire on June 30, 2004. It is the
Company's intention to extend the lease of these facilities.
Beginning in January 2004, the Company began leasing additional
adjacent space at annual rental rate of $15,562.
The Company believes our manufacturing, warehouse and office facilities are
suitable and adequate and afford sufficient capacity for our current and
reasonably foreseeable future needs. The Company believes it has adequate
insurance coverage for our properties and their contents.
ITEM 3. LEGAL PROCEEDINGS
None.
ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS
None.
16
PART II
ITEM 5. MARKET FOR REGISTRANT'S COMMON EQUITY AND RELATED STOCKHOLDER MATTERS
AND ISSUER PURCHASES OF EQUITY SECURITIES
Price Range of Common Stock
The Company's common stock, par value $.02 per share ("Common Stock"), is traded
on the over-the-counter market with quotations reported on the National
Association of Securities Dealers Automated Quotation System (NASDAQ) under the
symbol GAIT. The following table sets forth the high and low closing bid prices
for the Common Stock for the year ended December 31, 2003 and December 31, 2002.
The NASDAQ quotations represent prices between dealers, do not include retail
markups, markdowns or commissions, and may not represent actual transactions.
Year ended December 31, 2003 High Low
--------------------------------------------- -------- --------
Three months ended March 31, 2003 $ 3.77 $ 2.99
Three months ended June 30, 2003 $ 3.40 $ 2.55
Three months ended September 30, 2003 $ 3.50 $ 3.10
Three months ended December 31, 2003 $ 3.50 $ 2.85
Year ended December 31, 2002 High Low
--------------------------------------------- -------- --------
Three months ended March 31, 2002 $ 8.30 $ 7.11
Three months ended June 30, 2002 $ 8.25 $ 5.90
Three months ended September 30, 2002 $ 6.43 $ 4.50
Three months ended December 31, 2002 $ 5.25 $ 3.51
The closing price on March 17, 2004 was $6.19. On March 17, 2004, there were
approximately 247 holders of record of the Common Stock. However, this figure is
exclusive of all owners whose stock is held beneficially or in "street" name.
Based on information supplied by various securities dealers, the Company
believes that there are in excess of 247 shareholders in total, including
holders of record and beneficial owners of shares held in "street" name.
Dividend History and Policy
The Company did not pay cash dividends on its Common Stock in 2003, 2002 and
2001 and anticipates that, for the foreseeable future, it will follow a policy
of utilizing retained earnings, if any, to finance the expansion and development
of its business. In any event, future dividend policy will depend upon the
Company's earnings, financial condition, working capital requirements and other
factors.
17
Recent Sales of Unregistered Securities
Described below is information regarding securities the Company issued in the
year ended December 31, 2003 which were not registered under the Securities Act
of 1933.
In January 2003, the Company completed the acquisition of Bi-Op. In connection
with the acquisition, the Company issued 107,611 shares of the Company's common
stock.
The Company issued 3,096 shares of the Company's common stock to one of its
medical directors as compensation for services on October 13, 2003. The closing
price of the stock on such date was $3.40.
The above sales were private transactions not involving a public offering and
were exempt from the registration provisions of the Securities Act pursuant to
Section 4(2) thereof. No underwriter was engaged in connection with the
foregoing sales of securities. The Company has reason to believe that: (i) all
of the foregoing purchasers were familiar with or had access to information
concerning the Company's operations and financial condition, and (ii) all of
those individuals purchasing securities represented that they acquired the
shares for investment and not with a view to the distribution thereof.
18
ITEM 6. SELECTED FINANCIAL DATA
Ten months Years ended
Year ended Year ended ended -------------------
(in thousands, except per share data) Dec. 31, Dec. 31, Dec. 31, Feb. 28, Feb. 29,
2003 2002 2001 2001 2000
------ ------ ------ ------ ------
$ $ $ $ $
Consolidated Statement of Operations
Net sales 24,721 18,677 10,936 12,072 11,572
Change in control and restructuring expenses -- -- -- (1,008) --
Operating profit (loss) 764 (470) 139 (1,504) (356)
Income (loss) before income taxes 161 (998) 73 (1,502) (337)
Net (loss) income (5) (1,106) 70 (1,506) (335)
Net income (loss) per common share:
Basic -- (.26) .02 (.58) (.13)
Diluted -- (.26) .02 (.58) (.13)
Weighted average number of common shares:
Basic 4,374 4,246 3,860 2,583 2,571
Diluted 4,374 4,246 4,307 2,583 2,571
Dec. 31, Dec. 31, Dec. 31, Feb. 28, Feb. 29,
2003 2002 2001 2001 2000
------- ------- ------- ------- -------
$ $ $ $ $
Consolidated Balance Sheets:
Working capital 7,434 10,569 16,655 757 1,715
Total assets 24,023 23,810 20,700 4,554 4,738
Long-term liabilities
(excluding current maturities) 15,528 15,937 14,719 126 277
Stockholders' equity 3,775 3,112 3,866 1,599 2,536
19
ITEM 7. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS
OF OPERATIONS
The following discussion and analysis should be read in conjunction with the
financial statements and notes thereto of the Company which are included in Item
8.
Executive Summary:
Our Business
The Company's revenues are generated from the sale of orthopedic products in the
United States, Canada and the United Kingdom. The Company specializes in
designing, manufacturing, distributing, and marketing high quality orthotic and
gait-related products. Such products include both custom orthotic devices and
pre-fabricated orthopedic rehabilitation and recovery devices. The Company's
largest expenses are cost of goods sold (which included fabricated products and
purchased goods), selling expenses and general and administrative expenses.
Since January 1, 2002, the Company has operated in two segments, custom
orthotics and distributed products.
Custom Orthotics
The Company's custom orthotic devices are contoured molds, purchased by a
healthcare professional for a patient, which are worn in the shoe to correct
biomechanical foot and postural disorders in patients which often result in pain
or discomfort, or otherwise impede an individual's ability to maintain a normal
gait. The Company also provides custom devices which support or control the
ankle region (ankle foot orthosis).
Distributed Products
The Company's distributed products are manufactured by others and consist of;
(i) prefabricated products for the lower extremities and (ii) a selection of
therapeutic footware. These products, which supplement our custom orthotic
product line, consist of modular shoe inserts, ankle braces, compression hose,
socks, and therapeutic shoes and sneakers, and are purchased by healthcare
professionals for use by their patients. In addition, we distribute PPT(R) to
manufacturers who incorporate PPT(R) into their products. PPT(R) is a soft
tissue cushioning material made from medical grade urethane produced in
laminated sheet form, molded insoles, and components for orthotic devices.
Recent Acquisitions:
As described in Note 2 of Notes to Consolidated Financial Statements, in 2002
and 2003, the Company acquired Benefoot, Inc. and Benefoot Professional
Products, Inc. (jointly "Benefoot") and Bi-Op Laboratories, Inc. ("Bi-Op).
Company Strategy:
The Company continues to seek and develop products that will increase the
Company's margins. Management has introduced technology to improve the
manufacturing process, increase quality and improve efficiences. Further the
Company will look for synergistic acquisition candidates that improve the
Company's profitability either by adding products, distribution networks or new
markets.
The Company is in a highly competitive industry and competes with companies with
lower cost structures. The Company has or intends to increase the prices of
certain of its orthotic devices which may negatively impact volume. The Company
believes that any loss in volume will be offset in the Company's overall gross
profit by the price changes and the focus on more profitable products.
20
Critical Accounting Policies and Estimates
The Company's accounting policies are more fully described in Note 1 of Notes to
Consolidated Financial Statements. The preparation of financial statements in
conformity with accounting principles generally accepted in the United States of
America requires management to make estimates and assumptions that affect the
reported amounts of assets and liabilities and disclosure of contingent assets
and liabilities at the date of the financial statements and the reported amounts
of revenues and expenses during the reporting period. Future events and their
effects cannot be determined with absolute certainty. Therefore, the
determination of estimates requires the exercise of judgment. Actual results may
differ from these estimates under different assumptions or conditions.
Management believes the most significant accounting estimates inherent in the
preparation of the Company's consolidated financial statements include estimates
associated with its determination of liabilities related to warranty activity
and estimates associated with the Company's reserves with respect to
collectibility of accounts receivable, allowances for sales returns, inventory
valuations, and valuation allowance for deferred tax assets. Various assumptions
and other factors underlie the determination of these significant estimates. The
process of determining significant estimates is fact specific and takes into
account factors such as historical experience, current and expected economic
conditions, and product mix. The Company constantly re-evaluates these
significant factors and makes adjustments where facts and circumstances dictate.
Historically, actual results have not significantly deviated from those
determined using the estimates described above.
The warranty reserve at December 31, 2002 was $70,000. During the year ended
December 31, 2003, the Company added $404,000 to the reserve and charged
$404,000 against the reserve for costs incurred to complete warranty repairs.
The warranty reserve at December 31, 2003 was $70,000. If future costs incurred
were to differ from our estimates, we may need to increase or decrease our
reserve.
The allowance for doubtful accounts at December 31, 2002 was $124,935. During
the year ended December 31, 2003 the Company added $117,993 to the allowance
based upon increased net sales and its review of the accounts receivable aging.
The Company wrote off or recovered $18,203 in uncollectible accounts. The
allowance for doubtful accounts at December 31, 2003 was $224,725. If future
payments by our customers were different from our estimates, we may need to
increase or decrease our allowance for doubtful accounts.
The sales returns and allowances at December 31, 2002 were $28,000. During the
year ended December 31, 2003 the Company added $40,000 in current expense
charges to the allowance based upon the increased net sales and its review of
sales return and allowance trends during the year. The sales returns and
allowances at December 31, 2003 were $68,000. If actual sales returns and
allowances were to differ from our estimates, we may need to increase or
decrease our sales return and allowance.
The inventory reserve for excess or obsolete inventory at December 31, 2002 was
$220,405. During the year ended December 31, 2003 the Company added $129,063 of
additional reserves and wrote off $39,468 in excess or obsolete inventory which
was disposed of during the year. The Company reviewed its inventory levels and
aging relative to current and expected usage and determined the requirement for
additions to the reserve. The inventory reserve for obsolete inventory at
December 31, 2003 was $310,000. If the inventory quality or usage relative to
quantities held was to deteriorate or improve in the future, we may need to
increase or decrease our reserve for excess or obsolete inventory
21
The valuation allowance relating to deferred tax assets was $2,408,241 at
December 31, 2002 which represented a full allowance against all net deferred
tax assets except approximately $6,000 related to an alternate minimum tax
carryforward. During the year ended December 31, 2003, the valuation allowance
increased by $16,768 to $2,425,009 at December 31, 2003. The Company believes
this valuation allowance is required because it is more likely than not that
these deferred tax assets will not be recognized.
Results of Operations:
The following table presents the results for the year ended December 31, 2003,
the comparable results for the year ended December 31, 2002 and the unaudited
pro forma results for the year ended December 31, 2001. For comparative purposes
the unaudited pro forma results of operations for the twelve months ended
December 31, 2001 have been derived from the previously reported results for the
ten months ended December 31, 2001 plus the results for the two months ended
February 28, 2001, and are unaudited.
Years ended
--------------------------------------------
December 31, December 31, December 31,
2003 2002 2001
------------ ------------ ------------
(unaudited)
(pro forma)
Net sales $ 24,720,515 $ 18,676,503 $ 12,782,366
Cost of sales 16,049,790 11,962,104 8,503,020
------------ ------------ ------------
Gross profit 8,670,725 6,714,399 4,279,346
General and administrative expenses 4,775,142 3,867,882 2,768,134
Selling expenses 3,131,197 3,151,205 1,623,259
Research and development expenses -- 164,872 182,497
Change in control expenses -- -- 795,667
------------ ------------ ------------
Income (loss) from operations 764,386 (469,560) (1,090,211)
------------ ------------ ------------
Other income (expense):
Interest income 157,522 214,481 86,614
Interest expense (836,273) (829,498) (143,394)
Other 75,798 86,214 (11,669)
------------ ------------ ------------
Other income (expense), net (602,953) (528,803) (68,449)
------------ ------------ ------------
Income (loss) before income taxes 161,433 (998,363) (1,158,660)
Provision for income taxes 166,904 107,294 3,118
------------ ------------ ------------
Net loss $ (5,471) $ (1,105,657) $ (1,161,778)
============ ============ ============
2003 compared to 2002
Net loss for the year ended December 31, 2003 ("2003") was $5,471 as compared to
a loss of $1,105,657 for the year ended December 31, 2002 ("2002"). The
principal reason for the decrease in the loss was the increase in net sales and
gross profit partially offset by an increase in general and administrative
expenses both of which are described below.
Net sales for 2003 were $24,720,515 as compared to $18,676,503 in 2002, an
increase of $6,044,012 or 32.4%.
Net sales of custom orthotics increased $4,447,061 or 30.3% to $19,115,633 in
2003 from $14,668,572 in 2002. This increase was primarily due to an increase in
domestic custom othotics of $2,123,878 which reflected a full year of operations
from the Benefoot acquisition which occurred in May 2002, net sales associated
with Bi-Op of
22
$1,624,172 which was acquired in January 2003 and increased sales of custom
orthotics in the United Kingdom of approximately $300,000.
Net sales of distributed products increased by $1,596,951 or 39.8% to $5,604,882
in 2003 from $4,007,931 in 2002. This increase was primarily attributable to a
full year of operations from the Benefoot acquisition which occurred in May
2002.
Consolidated gross profit decreased from 35.0% in 2002 to 35.1% in 2003 due to
decreases in gross profit percentages in both operating segments. Custom
orthotics gross profit percentage decreased slightly in 2002 as compared to 2003
primarily due to an increase in direct labor costs in the U.K. Distributed
products gross profit decreased slightly as well in 2002 as compared to 2003
primarily due to a change in product mix.
General and administrative expenses were $4,775,142 or 19.3% of net sales in
2003 as compared to $3,867,882 or 20.7% of net sales in 2002. The increase in
general and administrative expenses was attributable the amounts associated with
Bi-Op which was acquired in January 2003 (approximately $275,000) as well as an
increase in legal and professional fees required with respect to the Company's
regulatory compliance, an increase provision for the Company's incentive plan,
an increase in insurance costs, principally workers compensation and an increase
in pension expense. The decrease in general and administrative expenses as a
percentage of sales was primarily related to efficiencies created through the
leverage of Langer's infrastructure and the integration of Benefoot.
In 2003, the Company did not incur any research and development expenses; in
2002 such amounts were $164,872.
Selling expenses were $3,131,197 or 12.6% of net sales for the year ended
December 31, 2003 as compared to $3,151,205 or 16.9% of net sales for the year
ended December 31, 2002. The principal reason for the decrease as a percentage
of net sales basis, was the synergies created by the Benefoot acquisition which
provided a larger sales base with more products.
Other income (expenses) was ($602,953) in 2003 as compared to ($528,803) in
2002. Interest expense, which is substantially related to fixed rate debt, was
consistent in 2003 as compared to 2002 based upon the amount of indebtedness
outstanding. Interest income decreased by $56,959, from $214,481 to $157,522, or
27% in 2003 as compared to 2002 due to a decrease in the amount available for
investment in short term interest bearing accounts.
The provision for income taxes increased to $166,904 in 2003 from $107,294 in
2002. Prior to the adoption of SFAS No. 142, the Company would not have needed a
valuation allowance for the portion of the net operating losses equal to the
amount of tax-deductible goodwill and trade names amortization expected to occur
during the carryforward period of the net operating losses based on the timing
of the reversal of these taxable temporary differences. As a result of the
adoption of SFAS 142, the reversal will not occur during the carryforward period
of the net operating losses. Therefore, the Company recorded a deferred income
tax expense of approximately $158,000 and $82,000 during the years ended
December 31, 2003 and 2002 which would not have been required prior to the
adoption of SFAS 142. The deferred income tax recorded in 2003 was partially
offset by the recognition of a deferred tax benefit of approximately $6,000
related to an alternative minimum tax carryforward. Additionally, the Company's
foreign tax provision decreased to $119 in 2003 from $25,294 in 2002 because the
Company had pre-tax losses from foreign operations in 2003.
2002 Compared to 2001(unaudited pro forma)
The net loss for 2002 was $1,105,657 as compared to $1,161,778 for the unaudited
pro forma twelve month period ended December 31, 2001 ("2001 Period"). Below is
a discussion of the comparative results for these periods.
23
Net sales for 2002 were $18,676,504 as compared to $12,782,366 for the 2001
Period, an increase of $5,894,137 or approximately 46%. This increase was
primarily due to net sales attributable to the Benefoot acquisition which closed
on May 6, 2002 were approximately $4,899,000 in 2002.
Net sales of custom orthotic products were $14,668,572 in 2002 as compared to
$11,422,835 in the 2001 Period which is an increase of $3,145,737 or
approximately 28%. $2,702,000 of this increase was attributable to the Benefoot
acquisition.
Net sales of distributed products increased by $2,648,400 in 2002 to $4,007,931
as compared to $1,359,531 for the 2001 Period. $2,197,000 of the increase was
attributable to nets sales related to the Benefoot acquisition and approximately
$451,000 was the result of organic growth in the sales of PPT(R) and other
distributed products.
Gross profit in 2002 was 35.9% as compared to 33.5% for the 2001 Period. Gross
profit improved primarily as the result of improvement in efficiencies in the
manufacturing process, reduction in overhead costs and increased sales.
Selling expense increased in 2002 to $3,151,205 or 16.8% of net sales in 2002 as
compared to $1,623,259 or 12.7% of net sales for the 2001 Period due to the
effect of the Benefoot acquisition, increases in related payroll and investments
made in improving the sales and marketing infrastructure.
General and administrative expenses were $3,867,882 or 20.7% of net sales in
2002 as compared to $2,768,134 or 21.7% of net sales for the 2001 Period. The
increase was due to a management commitment to strengthen the Company's
infrastructure as well as amortization associated with certain identifiable
intangible asset acquired in 2002.
Research and development was $164,872 in 2002 as compared to $182,497 in the
2001 Period which was consistent with the Company's level of activity.
Other income (expense) was $(528,803) in 2002 as compared to $(68,422) for the
2001 Period. The principal reason for the increase was interest (including
amortization of debt issuance costs) relating to the 4% convertible notes which
were issued in October 2001 and were outstanding for all of 2002, partially
offset by interest income earned on unutilized proceeds.
The provision for income taxes increased to $107,294 in 2002 from $3,118 in the
2001 Period. Prior to the adoption of SFAS No. 142, the Company would not have
needed a valuation allowance for the portion of the net operating losses equal
to the amount of tax-deductible goodwill and trade names amortization expected
to occur during the carryforward period of the net operating losses based on the
timing of the reversal of these taxable temporary differences. As a result of
the adoption of SFAS 142, the reversal will not occur during the carryforward
period of the net operating losses. Therefore, the Company recorded a deferred
income tax expense of approximately $82,000 during the year ended December 31,
2002 which would not have been required prior to the adoption of SFAS 142. This
issue did not effect the Company's provision for income taxes in the 2001
period. Additionally, the Company's foreign tax provision increased to $25,204
in 2002 from $10,683 in the 2001 Period due to increased pre-tax earnings from
foreign operations.
Liquidity and Capital Resources
Working capital as of December 31, 2003 was $7,433,951 as compared to
$10,568,549 at December 31, 2002. Cash balances at December 31, 2003 were
$5,533,946, a decrease of $3,877,764 from December 31, 2002. The primary reason
for the decrease in cash and working capital in 2003 were: (1) the Company's
$1,897,328 investments in business, net of cash acquired, (2) the Company's
$1,402,336 purchase of property and equipment including $1.1 million relating to
the installation and implementation of a new information technology system.
24
Long-term Debt
On October 31, 2001, the Company sold 14,589,000 of its 4% convertible
subordinated notes, due August 31, 2006, in a private placement (the "Notes").
The Notes are convertible into the Company's common stock at a conversion price
of $6.00 per share and are subordinated to all existing or future senior
indebtedness of the Company. The Company received net proceeds of $13,668,067
from this offering. The costs of raising these proceeds, including placement and
legal fees, was $920,933, which is being amortized over the life of the Notes.
The amortization of these costs for the years ended December 31, 2003 and 2002
was $193,772 and $193,105, respectively. Cash paid for interest is payable
semi-annually on the last date in June and December. Cash payments for interest
expense for each of the years ended December 31, 2003 and 2002 on these Notes
was $583,560.
The Company issued $1,800,000 in 4% promissory notes ("Benefoot Notes") in
connection with the acquisition of Benefoot. $1,000,000 of the Benefoot Notes
were paid on May 6, 2003 and the balance is due on May 6, 2004. Interest expense
with respect to the Benefoot Notes was $45,932 and $47,200 in 2003 and 2002,
respectively.
25
Contractual Obligations
Certain of the Company's facilities and equipment are leased under
noncancellable operating leases. Additionally, as discussed above, the Company
has certain long-term and short-term indebtedness. The following is a schedule,
by fiscal year, of future minimum rental payments required under current
operating leases and debt repayment requirements as of December 31, 2003:
2004 2005 2006 2007
----------- ----------- ----------- -----------
Operating lease obligations amount $ 501,000 $ 216,000 $ 14,000 $ 9,000
Current and long term portion of notes
payable 800,000 -- 14,589,000 --
----------- ----------- ----------- -----------
Total Contractual Obligations (1)(2) $ 1,301,000 $ 216,000 $14,603,000 $ 9,000
=========== =========== =========== ===========
(1) The Company has no purchase commitments at December 31, 2003 other
than those incurred in the normal course of business.
(2) Other long term liabilities include unearned revenue (see Note 1(d)
to the Notes to the Consolidated Financial Statements), accrued
pension costs (see Note 11 to the Notes of the Consolidated
Financial Statements), and deferred tax liabilities included in
other liabilities on the Consolidated Balance Sheets (see Note 12 to
the Notes of the Consolidated Financial Statements)
The Company may finance acquisitions of other companies or product lines in the
future from existing cash balances, from borrowings from institutional lenders,
and/or the public or private offerings of debt or equity securities.
The Company is obligated to make the final payment under the Benefoot Notes
which total $800,000 plus interest in May 2004 and must pay additional
contingent purchase price payments, $302,000 of which has accrued at December
31, 2003. Additionally, the Company has paid or expects to pay approximately
$400,000 in 2004 to complete its information technology system conversion. The
Company believes it has sufficient working capital to meet its spending needs
for the next twelve months.
In 2003, the Company did not have earnings after taxes. To the extent that the
Company is unable to increase its profitability in the next two years it will
not have sufficient funds to repay its obligation under the convertible notes
which mature in 2006. The Company would have to refinance or restructure such
convertible notes at that time.
In 2003 the Company's United Kingdom subsidiary ("UK Subsidiary") maintained a
line of credit with a local bank in the amount of 50,000 British pounds, which
is guaranteed by the Company pursuant to a standby Letter of Credit. The Letter
of Credit expired in February 2004 and the Company thereafter provided
sufficient funds to the UK Subsidiary to meet its working capital requirements.
Inflation
The Company has in the past been able to increase the prices of its products or
reduce overhead costs sufficiently to offset the effects of inflation on wages,
materials and other expenses, and anticipates that it will be able to continue
to do so in the future.
26
Recently Issued Accounting Pronouncements
In August 2001, the Financial Accounting Standards Board ("FASB") issued SFAS
No. 143, "Accounting for Asset Retirement Obligations." This standard requires
entities to record the fair value of a liability for an asset retirement
obligation in the period in which it is incurred. When the liability is
initially recorded, the entity capitalizes a cost by increasing the carrying
amount of the related long-lived asset. Over time the liability is accreted to
its present value each period and the capitalized cost is depreciated over the
useful life of the related asset. Upon settlement of the liability, an entity
either settles the obligation for its recorded amount or incurs a gain or loss
upon settlement. The standard is effective for fiscal years beginning after June
15, 2002. The adoption of SFAS No. 143 did not have a material impact on the
Company's consolidated financial statements.
In April 2002, the FASB issued SFAS No. 145, "Rescission of FASB Statements No.
4, 44 and 64, Amendment of FASB Statement No. 13, and Technical Corrections."
SFAS No. 145, among other things, rescinds SFAS No. 4, which required all gains
and losses from the extinguishment of debt to be classified as an extraordinary
item and amends SFAS No. 13 to require that certain lease modifications that
have economic effects similar to sale-leaseback transactions be accounted for in
the same manner as sale-leaseback transactions. The rescission of SFAS No. 4 is
effective for fiscal years beginning after May 15, 2002. The remainder of the
statement is generally effective for transactions occurring after May 15, 2002
with earlier application encouraged. The adoption of SFAS No.145 did not have a
material impact on the Company's consolidated financial statements.
In June 2002, the FASB issued SFAS No. 146, "Accounting for Exit or Disposal
Activities." This statement addresses the recognition, measurement and reporting
of costs that are associated with exit and disposal activities. This statement
includes the restructuring activities that are currently accounted for pursuant
to the guidance set forth in EITF 94-3, "Liability Recognition for Certain
Employee Termination Benefits and other Costs to exit an Activity (including
Certain Costs Incurred in a Restructuring)," costs related to terminating a
contract that is not a capital lease and one-time benefit arrangements received
by employees who are involuntarily terminated- nullifying the guidance under
EITF 94-3. Under SFAS No. 146 the cost associated with an exit or disposal
activity is recognized in the periods in which it is incurred rather than at the
date the company committed to the exit plan. This statement is effective for
exit or disposal activities initiated after December 31, 2002 with earlier
application encouraged. The adoption of SFAS No. 146 did not have a material
effect on the Company's consolidated financial statements.
In November 2002, the FASB issued Financial Interpretation ("FIN") 45,
"Guarantor's Accounting and Disclosure Requirements for Guarantees, Including
Indirect Guarantees of Indebtedness of Others." FIN 45 requires that the
guarantor recognize, at the inception of certain guarantees, a liability for the
fair value of the obligation undertaken in issuing such guarantee. FIN 45 also
requires additional disclosure requirements about the guarantor's obligations
and under certain guarantees that it has issued. The initial recognition and
measurement provisions of this interpretation are applicable on a prospective
basis to guarantees issued or modified after December 31, 2002. The disclosure
requirements of this interpretation are effective for financial statement
periods ending after December 15, 2002. The Company has included the required
disclosures under FIN 45 in the notes to the consolidated financial statements.
The adoption of the recognition and measurement provisions of FIN 45 did not
have a material effect on the Company's consolidated financial statements.
In January 2003 and revised in December 2003, the FASB issued FIN 46,
"Consolidation of Variable Interest Entities, an Interpretation of Accounting
Research Bulletin No. 51 and an amendment to FIN 46 entitled FASB Interpretation
No. 46 (revised December 2003), Consolidation of Variable Interest Entities
("FIN 46R"). FIN 46R requires certain variable interest entities to be
consolidated by the primary beneficiary of the entity if the equity investors in
the entity do not have the characteristics of a controlling financial interest
or do not have sufficient equity at risk for the entity to finance its
activities without additional subordinated financial support form other parties.
FIN 46R will be applied by the Company to those entities that are considered
variable interest entities as of March 31, 2004. The Company does not expect
that the adoption of FIN 46R will have a material effect on its consolidated
financial statements.
27
In April 2003, the FASB issued SFAS No. 149, "Amendment of Statement 133 on
Derivative Instruments and Hedging Activities." SFAS No. 149 amends and
clarifies accounting for derivative instruments, including certain derivative
instruments embedded in other contracts, and for hedging activities under SFAS
No. 133, "Accounting for Derivative Instruments and Hedging Activities." SFAS
No. 149 is generally effective for derivative instruments, including derivative
instruments embedded in certain contracts, entered into or modified after June
30, 2003 and for hedging relationships designated after June 30, 2003. The
adoption of SFAS No. 149 did not have a material effect on the Company's
consolidated financial statements.
In May 2003, the FASB issued SFAS No. 150, "Accounting for Certain Financial
Instruments with Characteristics of both Liabilities and Equity." SFAS No. 150
establishes standards for how to classify and measure certain financial
instruments with characteristics of both liabilities and equity. The statement
is effective for financial instruments entered into or modified after May 31,
2003. The adoption of SFAS No. 150 did not have a material impact on the
Company's consolidated financial statements.
In December 2003, the FASB issued SFAS No. 132, as revised, Employers'
Disclosures about Pensions and Other Postretirement Benefits, ("Revised SFAS
132"), which requires additional disclosures about assets, obligation, cash
flows, and net periodic benefit cost of defined benefit pension plans and other
defined benefit postretirement plans. The Company adopted the required revised
disclosure provisions of Revised SFAS 132 as of December 31, 2003, except for
the disclosure of estimated future benefit payments, which the Company is
required to and will disclose as of December 31, 2004.
28
Certain Factors That May Affect Future Results
Information contained or incorporated by reference in the annual report on Form
10-K, in other SEC filings by the Company, in press releases, and in
presentations by the Company or its management, contains "forward-looking
statements" within the meaning of the Private Securities Litigation Reform Act
of 1995 which can be identified by the use of forward-looking terminology such
as "believes," "expects," "plans," "intends," "estimates," "projects," "could,"
"may," "will," "should," or "anticipates" or the negatives thereof, other
variations thereon or comparable terminology, or by discussions of strategy. No
assurance can be given that future results covered by the forward-looking
statements will be achieved, and other factors could also cause actual results
to vary materially from the future results covered in such forward-looking
statements. Such forward-looking statements include, but are not limited to,
those relating to the Company's financial and operating prospects, future
opportunities, the Company's acquisition strategy and ability to integrate
acquired companies and assets, outlook of customers, and reception of new
products, technologies, and pricing. In addition, such forward-looking
statements involve known and unknown risks, uncertainties, and other factors
which may cause the actual results, performance or achievements of the Company
to be materially different from any future results expressed or implied by such
forward-looking statements. Also, the Company's business could be materially
adversely affected and the trading price of the Company's common stock could
decline if any such risks and uncertainties develop into actual events. The
Company undertakes no obligation to publicly update or revise forward-looking
statements to reflect events or circumstances after the date of this Form 10-K
or to reflect the occurrence of unanticipated events.
29
ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
In general, business enterprises can be exposed to market risks, including
fluctuation in commodity and raw materials prices, foreign currency exchange
rates, and interest rates that can adversely affect the cost and results of
operating, investing, and financing. In seeking to minimize the risks and/or
costs associated with such activities, the Company manages exposure to changes
in commodities and raw material prices, interest rates and foreign currency
exchange rates through its regular operating and financing activities. The
Company does not utilize financial instruments for trading or other speculative
purposes, nor does the Company utilize leveraged financial instruments or other
derivatives. The following discussion about our market rate risk involves
forward-looking statements. Actual results could differ materially from those
projected in the forward-looking statements.
The Company's exposure to market rate risk for changes in interest rates relates
primarily to the Company's short-term monetary investments. There is a market
rate risk for changes in interest rates earned on short-term money market
instruments. There is inherent rollover risk in the short-term money market
instruments as they mature and are renewed at current market rates. The extent
of this risk is not quantifiable or predictable because of the variability of
future interest rates and business financing requirements. However, there is no
risk of loss of principal in the short-term money market instruments, only a
risk related to a potential reduction in future interest income. Derivative
instruments are not presently used to adjust the Company's interest rate risk
profile.
The majority of the Company's business is denominated in United States dollars.
There are costs associated with the Company's operations in foreign countries,
primarily the United Kingdom and Canada, which require payments in the local
currency and payments received from customers for goods sold in these countries
are typically in the local currency. The Company partially manages its foreign
currency risk related to those payments by maintaining operating accounts in
these foreign countries and by having customers pay the Company in those same
currencies.
30
ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTAL DATA
LANGER, INC. AND SUBSIDIARIES
Index to Consolidated Financial Statements and Schedule II
PAGE
----
Independent Auditors' Report 32
Consolidated Financial Statements:
Consolidated Balance Sheets 33
Consolidated Statements of Operations 34
Consolidated Statements of Stockholders' Equity 35
Consolidated Statements of Cash Flows 36
Notes to Consolidated Financial Statements 37
Consolidated Financial Statement Schedule II -
Valuation and Qualifying Accounts 60
All other schedules have been omitted because they are not applicable, not
required or the information is disclosed in the consolidated financial
statements, including the notes thereto.
31
INDEPENDENT AUDITORS' REPORT
To the Stockholders and Board of Directors of
Langer, Inc. and Subsidiaries
We have audited the accompanying consolidated balance sheets of Langer, Inc. and
subsidiaries (the "Company") as of December 31, 2003 and 2002, and the related
consolidated statements of operations, stockholders' equity and cash flows for
the years ended December 31, 2003 and 2002, and for the ten months ended
December 31, 2001. Our audits also included the financial statement schedules
listed in the foregoing index for the years ended December 31, 2003 and 2002,
and for the ten months ended December 31, 2001. These consolidated financial
statements and financial statement schedules are the responsibility of the
Company's management. Our responsibility is to express an opinion on the
consolidated financial statements and financial statement schedules based on our
audits.
We conducted our audits in accordance with auditing standards generally accepted
in the United States of America. Those standards require that we plan and
perform the audit to obtain reasonable assurance about whether the consolidated
financial statements are free of material misstatement. An audit includes
examining, on a test basis, evidence supporting the amounts and disclosures in
the consolidated financial statements. An audit also includes assessing the
accounting principles used and significant estimates made by management, as well
as evaluating the overall consolidated financial statement presentation. We
believe that our audits provide a reasonable basis for our opinion.
In our opinion, such consolidated financial statements present fairly, in all
material respects, the financial position of the Company at December 31, 2003
and 2002, and the results of its operations and its cash flows for the years
ended December 31, 2003 and 2002, and for the ten months ended December 31,
2001, in conformity with accounting principles generally accepted in the United
States of America. Also, in our opinion, such financial statement schedules,
when considered in relation to the basic consolidated financial statements taken
as a whole, presents fairly in all material respects the information set forth
therein.
DELOITTE & TOUCHE LLP
Jericho, New York
March 29, 2004
32
LANGER, INC.
AND SUBSIDIARIES
Consolidated Balance Sheets
December 31, December 31,
2003 2002
------------ ------------
Assets
Current assets:
Cash and cash equivalents $ 5,533,946 $ 9,411,710
Accounts receivable, net of allowances for doubtful
accounts and returns and allowances aggregating $292,725
and $152,935, respectively 3,628,052 2,937,340
Inventories, net 2,496,583 2,353,153
Prepaid expenses and other 495,386 627,154
------------ ------------
Total current assets 12,153,967 15,329,357
Property and equipment, net 2,496,071 943,893
Identifiable intangible assets, net 3,960,105 3,313,413
Goodwill 4,536,198 3,186,386
Other assets 876,856 1,037,105
------------ ------------
Total assets $ 24,023,197 $ 23,810,154
============ ============
Liabilities and stockholders' equity
Current liabilities:
Current maturities of long-term debt $ 800,000 $ 1,000,000
Accounts payable 1,133,149 1,235,598
Other current liabilities 2,114,270 1,864,344
Unearned revenue 672,597 660,866
------------ ------------
Total current liabilities 4,720,016 4,760,808
Long-term debt 14,589,000 15,389,000
Unearned revenue 166,757 162,455
Accrued pension expense 171,893 209,539
Other liabilities 600,338 176,138
------------ ------------
Total liabilities 20,248,004 20,697,940
------------ ------------
Stockholders' equity
Preferred stock, no par value; authorized 250,000 shares;
no shares issued -- --
Common stock, $.02 par value; authorized 50,000,000
shares; issued 4,447,451 and 4,336,744, respectively 88,949 86,735
Additional paid-in capital 13,202,129 12,825,237
Accumulated deficit (9,159,140) (9,153,669)
Accumulated other comprehensive loss (241,288) (530,632)
------------ ------------
3,890,650 3,227,671
Treasury stock at cost, 67,100 shares (115,457) (115,457)
------------ ------------
Total stockholders' equity 3,775,193 3,112,214
------------ ------------
Total liabilities and stockholders' equity $ 24,023,197 $ 23,810,154
============ ============
See accompanying notes to consolidated financial statements.
33
LANGER, INC. AND SUBSIDIARIES
Consolidated Statements of Operations
Ten months
Year ended Year ended ended
December 31, December 31, December 31,
2003 2002 2001
------------ ------------ ------------
Net sales $ 24,720,515 $ 18,676,503 $ 10,936,112
Cost of sales 16,049,790 11,962,104 6,934,402
------------ ------------ ------------
Gross profit 8,670,725 6,714,399 4,001,710
General and administrative expenses 4,775,142 3,867,882 2,425,177
Selling expenses 3,131,197 3,151,205 1,294,991
Research and development expenses -- 164,872 142,192
------------ ------------ ------------
Operating income (loss) 764,386 (469,560) 139,350
------------ ------------ ------------
Other income (expense):
Interest income 157,522 214,481 86,635
Interest expense (836,273) (829,498) (138,846)
Other 75,798 86,214 (13,742)
------------ ------------ ------------
Other expense, net (602,953) (528,803) (65,953)
------------ ------------ ------------
Income (loss) before income taxes 161,433 (998,363) 73,397
Provision for income taxes (Note 12) 166,904 107,294 3,118
------------ ------------ ------------
Net (loss) income $ (5,471) $ (1,105,657) $ 70,279
============ ============ ============
Weighted average number of common shares used in
computation of net (loss) income per share:
Basic 4,374,396 4,245,711 3,860,167
============ ============ ============
Diluted 4,374,396 4,245,711 4,306,536
============ ============ ============
Net (loss) income per common share:
Basic $ (.00) $ (.26) $ .02
============ ============ ============
Diluted $ (.00) $ (.26) $ .02
============ ============ ============
See accompanying notes to consolidated financial statements
34
LANGER, INC. AND SUBSIDIARIES
Consolidated Statements of Stockholders' Equity
Common Stock
-------------------------- Treasury Additional Accumulated
Shares Amount stock paid-in capital deficit
----------- ----------- ----------- --------------- -----------
Balance at March 1, 2001: 2,849,022 $ 56,981 $ (115,457) $ 10,086,555 $(8,118,291)
Net income for ten months
ended December 31, 2001 70,279
Foreign currency adjustment
Minimum pension liability
adjustment
Total comprehensive income
Issuance of stock 1,400,000 28,000 2,107,000
Exercise of stock options 19,000 380 30,183
Issuance of stock options for
consulting services 8,243
Compensation expense to
accelerate stock options 26,743
----------- ----------- ----------- --------------- -----------
Balance at December 31, 2001: 4,268,022 85,361 (115,457) 12,258,724 (8,048,012)
Net loss (1,105,657)
Foreign currency adjustment
Minimum pension liability
adjustment
Total comprehensive (loss)
Issuance of stock to purchase
business 64,895 1,298 528,214
Issuance of stock and exercise
of stock options 3,827 76 11,729
Issuance of stock options for
consulting services 6,513
Compensation expense to
accelerate stock options 20,057
----------- ----------- ----------- --------------- -----------
Balance at December 31, 2002 4,336,744 86,735 (115,457) 12,825,237 (9,153,669)
Net loss (5,471)
Foreign currency adjustment
Minimum pension liability
adjustment
Total comprehensive (loss)
Issuance of stock to purchase
business 107,611 2,152 366,954
Issuance of shares from
treasury
Issuance of stock for
consulting services 3,096 62 9,938
----------- ----------- ----------- --------------- -----------
Balance at December 31, 2003 4,447,451 $ 88,949 $ (115,457) $ 13,202,129 $(9,159,140)
Accumulated Other
Comprehensive Income
(Loss)
------------------------
Foreign Minimum Total
currency pension Comprehensive stockholders'
translation liability income equity
----------- --------- ------------- -------------
Balance at March 1, 2001: $ (52,734) $(257,723) $ 1,599,331
Net income for ten months
ended December 31, 2001 $ 70,279
Foreign currency adjustment (53) (53)
Minimum pension liability
adjustment (3,897) (3,897)
-------------
Total comprehensive income $ 66,329 66,329
=============
Issuance of stock 2,135,000
Exercise of stock options 30,563
Issuance of stock options for
consulting services 8,243
Compensation expense to
accelerate stock options 26,743
----------- --------- ------------- -------------
Balance at December 31, 2001: (52,787) (261,620) 3,866,209
Net loss $ (1,105,657)
Foreign currency adjustment 26,570 26,570
Minimum pension liability
adjustment (242,795) (242,795)
-------------
Total comprehensive (loss) $ (1,321,882) (1,321,882)
=============
Issuance of stock to purchase
business 529,512
Issuance of stock and exercise
of stock options 11,805
Issuance of stock options for
consulting services 6,513
Compensation expense to
accelerate stock options 20,057
----------- --------- ------------- -------------
Balance at December 31, 2002 (26,217) (504,415) 3,112,214
Net loss $ (5,471)
Foreign currency adjustment 238,038 238,038
Minimum pension liability
adjustment 51,306 51,306
-------------
Total comprehensive (loss) $ 283,873 283,873
=============
Issuance of stock to purchase
business 369,106
Issuance of shares from
treasury
Issuance of stock for
consulting services 10,000
----------- --------- ------------- -------------
Balance at December 31, 2003 $ 211,821 $(453,109) $ 3,775,193
See accompanying notes to consolidated financial statements.
35
LANGER, INC. AND SUBSIDIARIES
Consolidated Statements of Cash Flows
Ten months
Year ended Year ended ended
December 31, December 31, December 31,
2003 2002 2001
------------ ------------ ------------
Cash Flows From Operating Activities:
Net (loss) income $ (5,471) $ (1,105,657) $ 70,279
Adjustments to reconcile net income (loss) to net cash
(used in) provided by operating activities:
Depreciation and amortization 844,981 648,216 285,619
Compensation expense for options acceleration -- 20,057 26,743
Provision for doubtful accounts receivable 117,993 88,348 15,015
Deferred income taxes 135,500 79,606 7,227
Issuance of stock and stock options for consulting services 10,000 11,755 8,243
Changes in operating assets and liabilities:
Accounts receivable (512,078) (533,849) (116,976)
Inventories 33,901 (519,701) (166,021)
Prepaid expenses and other assets 403,361 (389,303) (963,332)
Accounts payable and other current liabilities (377,345) 359,524 (168,354)
Unearned revenue and other liabilities (200,723) (10,175) 28,416
------------ ------------ ------------
Net cash provided by (used in) operating activities 450,119 (1,351,179) (973,141)
------------ ------------ ------------
Cash Flows From Investing Activities:
Purchase of businesses, net of cash acquired (1,897,328) (4,703,606) --
Purchase of property and equipment (1,402,336) (333,697) (271,693)
------------ ------------ ------------
Net cash (used in) investing activities (3,299,664) (5,037,303) (271,6