Item 2. Management’s Discussion and Analysis
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.
The following discussion
and analysis of our financial condition and results of operations should be read in conjunction with our unaudited Condensed Financial
Statements and related notes thereto included in Part I, Item 1 of this Quarterly Report on Form 10-Q, and our audited financial
statements and related notes thereto included in Part II, Item 8 of our Annual Report on Form 10-K for the fiscal year ended June
30, 2022 (“fiscal 2022”).
Overview
Electromed, Inc. (“we,”
“our,” “us,” “Electromed” or the “Company”) develops and provides innovative airway
clearance products applying High Frequency Chest Wall Oscillation (“HFCWO”) technologies in pulmonary care for patients
of all ages.
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We manufacture, market and sell products that provide HFCWO, including
the SmartVest® Airway Clearance System (“SmartVest System”) that includes our newest generation SmartVest Clearway®
Airway Clearance System (“Clearway”), previous generations SmartVest SQL® and SV2100, and related products, to patients
with compromised pulmonary function. The SmartVest Clearway, which received 510(k) clearance from the U.S. Food and Drug Administration
in December 2022, offers a state-of-the-art patient experience with a simple touch screen user interface, remote monitoring of data, and
is the lightest HFCWO generator on the market. Clearway also includes SmartVest Connect™ wireless technology, which allows data
connection between physicians and patients to track therapy performance and collaborate in treatment decisions.
Our products are sold in both the
home health care market and the institutional market for use by patients in hospitals, which we refer to as “institutional sales.”
Since 2000, we have marketed the SmartVest System and its predecessor products to patients suffering from cystic fibrosis, bronchiectasis
and repeated episodes of pneumonia. Additionally, we offer our products to a patient population that includes neuromuscular disorders
such as cerebral palsy, muscular dystrophies, amyotrophic lateral sclerosis (“ALS”), the combination of emphysema and chronic
bronchitis commonly known as chronic obstructive pulmonary disease (“COPD”), and patients with post-surgical complications
or who are ventilator dependent or have other conditions involving excess secretion and impaired mucus transport.
The SmartVest System is often eligible
for reimbursement from major private insurance providers, health maintenance organizations (“HMOs”), state Medicaid systems,
and the federal Medicare system, which we believe is an important consideration for patients considering an HFCWO course of therapy. For
domestic sales, the SmartVest System may be reimbursed under the Medicare-assigned billing code (E0483) for HFCWO devices if the patient
has cystic fibrosis, bronchiectasis (including chronic bronchitis or COPD that has resulted in a diagnosis of bronchiectasis), or any
one of certain enumerated neuromuscular diseases, and can demonstrate that another less expensive physical or mechanical treatment did
not adequately mobilize retained secretions. Private payers consider a variety of sources, including Medicare, as guidelines in setting
their coverage policies and payment amounts.
Critical Accounting Estimates
For a description of our
critical accounting policies, estimates and assumptions used in the preparation of our financial statements, including the unaudited
Condensed Financial Statements in this Quarterly Report on Form 10-Q, see Note 1 to our unaudited Condensed Financial Statements
included in Part I, Item 1 of this Quarterly Report on Form 10-Q and Part II, Item 7, and Note 1 to our audited financial statements
included in Part II, Item 8, of our Annual Report on Form 10-K for fiscal 2022.
Some of our accounting
policies require us to exercise significant judgment in selecting the appropriate assumptions for calculating financial statements.
Such judgments are subject to an inherent degree of uncertainty and are based upon our historical experience, known trends in our
industry, terms of existing contracts, other information from outside sources, as appropriate and other factors. Therefore, management
discusses the development, selection and disclosures with the audit committee. Among other factors, these judgements are based
upon our historical experience, known trends in our industry, terms of existing contracts and other information from outside sources,
as appropriate. We believe the critical accounting policies that require the most significant estimates, assumptions and judgments
in the preparation of our financial statements, including the unaudited Condensed Financial Statements contained in this Quarterly
Report on Form 10-Q, include: revenue recognition and the estimation of variable consideration, inventory valuation, share-based
compensation and warranty reserve.
Impacts of COVID-19
on Our Business and Operations
In March 2020, the World
Health Organization designated COVID-19 as a global pandemic, and the U.S. Department of Health and Human Services designated COVID-19
as a public health emergency (“PHE”). In response to the COVID-19 pandemic and the U.S. federal government’s
declaration of a PHE, the Centers for Medicare & Medicaid Services (“CMS”) implemented a number of temporary rule
changes and waivers to allow prescribers to best treat patients during the period of the PHE. These waivers became effective on
March 1, 2020. Clinical indications and documentation typically required will not be enforced for respiratory-related products,
including the SmartVest System (solely with respect to Medicare patients). The minimum documentation now requires a valid order
and documentation of a respiratory-related diagnosis. Face-to-face and in-person requirements for respiratory devices are being
waived while the waiver is in place.
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On January 30, 2023, the
Biden administration announced that the COVID-19 national and PHE declarations will end on May 11, 2023 (the “PHE End Date”).
Without further action from the U.S. federal government, we expect the CMS waiver will terminate no later than the PHE End Date
and we may experience a one-time delay in some percentage of our Medicare net revenue as we expect our average Medicare patient
referral to approval timeframe will extend to pre-COVID-19 timeframes and referrals with diagnoses not covered pre-COVID-19 may
be cancelled or need to be submitted to CMS for an appeal. We are executing our plans to attempt to mitigate the potential effects
on our future net revenue resulting from the likely termination of the CMS waiver by hiring additional employees to increase capacity
and minimize the average timeframe to convert a Medicare patient referral to approval and re-educating clinicians on Medicare requirements
for reimbursement of HFCWO.
Impacts of Certain Macro-Economic
Conditions and the Supply Chain on Our Business and Operations
We observed increased lead
times for certain components in our supply chain and increased material costs and shipping rates during the second half of fiscal
2022 and into the nine months ended March 31, 2023. The changes to our supply chain lead times resulted in a temporary interruption
that impacted product availability for certain customers beginning in September 2022 and continuing through March 2023. We anticipate
that these increased lead times and temporary interruption of supply have the potential to continue through the fourth quarter
of our fiscal year ending June 30, 2023 (“fiscal 2023”). If we are unable to procure components to meet our demand
or if we extend delivery lead-times to our customers, there may be an adverse impact to our revenue and, longer term, the potential
of market share losses. We are taking actions to expedite components and to identify and qualify alternate suppliers for certain
components to minimize any impact to our revenue and customer deliveries.
We expect that material costs and shipping
rates will remain elevated during the fourth quarter of fiscal 2023 and the first half of our fiscal year ending June 30, 2024 relating
to supply chain availability and inflationary trends in electronic components and may extend to other components. In certain instances,
we have purchased key electronic materials in advance to ensure adequate future supply and mitigate the risk of potential supply chain
disruptions. It is possible that these macro-economic conditions could have a greater adverse impact on our supply chain in the future,
including impacts associated with preventative and precautionary measures taken by other businesses and applicable governments. A reduction
or further interruption in any of our manufacturing processes could have a material adverse effect on our business. Any significant increases
to our raw material or shipping costs could reduce our gross margins.
Results of Operations
Net Revenues
Net revenues for the
three and nine months ended March 31, 2023 and 2022 are summarized in the table below.
Three Months Ended
March 31,
Nine
Months Ended
March
31,
2023
2022
Increase (Decrease)
2023
2022
Increase (Decrease)
Home care
$ 10,971,000
$ 9,033,000
$ 1,938,000
21.5 %
$ 31,335,000
$ 27,721,000
$ 3,614,000
13.0 %
Institutional
440,000
392,000
48,000
12.2 %
1,420,000
1,174,000
246,000
21.0 %
Home care distributor
501,000
520,000
(19,000 )
(3.7 %)
1,391,000
1,063,000
328,000
30.9 %
International
156,000
196,000
(40,000 )
(20.4 %)
309,000
432,000
(123,000 )
(28.5 %)
Total
$ 12,068,000
$ 10,141,000
$ 1,927,000
19.0 %
$ 34,455,000
$ 30,390,000
$ 4,065,000
13.4 %
Home care revenue .
Home care revenue increased by $1,938,000, or 21.5%, for the three months ended March 31, 2023 compared to the same period in the prior year. For the nine months ended March 31, 2023, home care revenue was $31,335,000, representing an increase of $3,614,000, or 13.0%, compared to the same period in the prior year. The increase was primarily due to an increase in referrals and approvals. The increase in referrals was due to an increase in direct sales representatives as well as positive market momentum from the introduction of our newest generation SmartVest Clearway during the quarter and was partially offset by a temporary interruption in supply chain and associated operations in the nine months ended March 31, 2023.
The CMS waiver continues to benefit the non-commercial Medicare portion of our home care revenue by increasing the number of referrals and the approval percentage for non-covered diagnoses. We believe that our ongoing sales team execution, along with the continued return to pre-COVID-19 levels of patient face-to-face engagement with physicians and clinic access for our sales team and the recent introduction of our newest generation SmartVest Clearway, has the potential to mitigate much of the impact of the potential CMS waiver expiration. If we are unsuccessful in mitigating the impact of the CMS waiver expiration, we may experience a decrease in our historical year over year growth rate.
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Home care distributor
revenue . Home care distributor revenue decreased by $19,000, or 3.7%, for the three months ended March 31, 2023
compared to the same period in the prior year. For the nine months ended March 31, 2023, home care distributor revenue was $1,391,000,
an increase of $328,000, or 30.9%, compared to the same period in the prior year. Home care distributor sales are affected by the
timing of distributor purchases that can cause significant fluctuations in reported revenue on a quarterly basis. The year-to-date
revenue increase was due to increased demand from one of our primary home care distribution partners.
Institutional revenue.
Institutional revenue was $440,000, an increase of $48,000, or 12.2%, for the three months ended March 31, 2023 compared
to the same period in the prior year. For the nine months ended March 31, 2023, institutional revenue was $1,420,000, an increase
of $246,000, or 21.0%, compared to the same period in the prior year. The increase in the current year periods was primarily due
to increased consumable sales to institutional customers.
International revenue .
International revenue was $156,000, a decrease of $40,000, or 20.4%, for the three months ended March 31, 2023 compared to
the same period in the prior year. For the nine months ended March 31, 2023, international revenue was $309,000, a decrease of
$123,000, or 28.5%, compared to the same period in the prior year. International sales are affected by the timing of distributor
purchases that can cause significant fluctuations in reported revenue on a quarterly basis.
Gross profit
Gross profit increased to $9,056,000, or 75.0% of net revenues, for the three months ended March 31, 2023, from $7,743,000, or 76.4% of net revenues, in the same period in the prior year. Gross profit increased to $26,069,000, or 75.7% of net revenues, for the nine months ended March 31, 2023, from $23,324,000, or 76.7% of net revenues, in the same period in the prior year. The decrease in gross profit as a percentage of net revenues compared to the same period in the prior year was primarily due to increased material costs and component broker fees incurred to accelerate the ramp of supply for the Clearway product.
Operating expenses
Selling, general and
administrative expenses. Selling, general and administrative (“SG&A”) expenses were $7,694,000 and $22,937,000
for the three and nine months ended March 31, 2023, respectively, representing increases of $1,150,000 and $3,131,000, or 17.6%
and 15.8%, respectively, compared to the same periods in the prior year.
Payroll and compensation-related
expenses were $5,037,000 and $14,920,000 for the three and nine months ended March 31, 2023, respectively, representing increases
of $739,000 and $2,030,000, or 17.2% and 15.7%, respectively, compared to the same periods in the prior year. The increase in the
current year periods was primarily due to salaries and incentive compensation related to the higher average number of sales, sales
support, marketing, and reimbursement personnel to process higher patient referrals. We have also continued to provide regular
merit-based increases for our employees and are regularly benchmarking our compensation ranges for new and existing employees to
ensure we can hire and retain the talent needed to drive growth in our business. Field sales employees totaled 57 as of March 31,
2023, 48 of which were direct sales representatives, compared to 51 field sales employees and 42 direct sales representatives as
of March 31, 2022.
Travel, meals and entertainment
expenses were $658,000 and $2,290,000 for the three and nine months ended March 31, 2023, respectively, representing increases
of $20,000 and $390,000, or 3.1% and 20.5%, respectively, compared to the same periods in the prior year. The increase in the current
year periods was due to a higher average number of direct sales representatives as well as increases in airfare, lodging and inflationary
expenses for our annual sales meeting in August 2022.
Total discretionary marketing
expenses were $212,000 and $581,000 for the three and nine months ended March 31, 2023, respectively, representing decreases of
$29,000 and $24,000, or 12.0% and 4.0%, respectively, compared to the same periods in the prior year.
Professional fees were
$1,388,000 and $3,850,000 for the three and nine months ended March 31, 2023, respectively, representing increases of $382,000
and $646,000, or 38.0% and 20.2%, respectively, compared to the same periods in the prior year. Professional fees are primarily
for services related to legal costs, shareowner services and reporting requirements, information technology technical support and
consulting fees. The increase in the three months ended March 31, 2023 was primarily due to higher legal and consulting costs related
to the termination of the PHE and recruiting costs for multiple senior leadership positions, including a new Chief Executive Officer.
The additional increase in the nine months ended March 31, 2023 was primarily due to nonrecurring legal compliance fees of approximately
$400,000 for a reimbursement-related project offset by a reduction in expenses related to shareholder activism incurred during
the prior year, which concluded with a cooperation agreement that became effective in September 2021.
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Research and development
expenses . Research and development (“R&D”) expenses were $166,000 and $618,000 for the three and nine months
ended March 31, 2023, respectively, representing decreases of $170,000 and $423,000, or 50.6% and 40.6%, respectively, compared
to the same periods in the prior year. The decreases in R&D expenses to 1.4% and 1.8% of revenue for the three and nine months
ended March 31, 2023, respectively were due to the completion of the Clearway product development process, resulting in the full
launch to the U.S. home care market in March 2023.
Interest income, net
Net interest income for the three and nine months ended March 31, 2023 was $26,000 and $37,000, respectively, compared to $6,000 and $21,000, respectively, for the same periods in the prior year. These increases were due to a higher yield in our interest-bearing cash accounts.
Income tax expense
Income tax expense was estimated
at $147,000 and $418,000, and the effective tax rate was 14.7% and 16.4%, for the three and nine months ended March 31, 2023, respectively.
Estimated income tax expense for the three and nine months ended March 31, 2023 includes a discrete tax benefit of $176,000 and
$219,000, respectively, related to the exercise of stock options.
Income tax expense was estimated
at $224,000 and $576,000, and the effective tax rate was 25.8% and 23.1%, for the three and nine months ended March 31, 2022, respectively.
Estimated income tax expense for the three and nine months ended March 31, 2022 includes a discrete tax benefit of $22,000 and
$43,000, respectively, related to the exercise of stock options and other items.
Net income
Net income for the three and nine
months ended March 31, 2023 was $1,075,000 and $2,133,000, respectively, compared to $645,000 and $1,922,000 for the same periods in
the prior year. The increases in net income were driven primarily by revenue growth and a decrease in R&Dexpenses but partially
offset by increased SG&A expenses related to our sales and reimbursement investments to drive revenue growth as well as
increased material costs and broker fees incurred to ramp up supply for the Clearway product.
Liquidity and Capital Resources
Cash Flows and Sources of Liquidity
Cash Flows from Operating Activities
For the nine months ended
March 31, 2023, net cash provided by operating activities was $316,000. Cash flows provided by operating activities consisted of
net income of $2,133,000, non-cash expenses of $960,000, and a decrease in prepaid expenses and other assets of $105,000. These
cash flows from operating activities were offset by an increase in accounts receivable of $1,293,000, a decrease in accrued compensation
of $660,000, an increase in income tax receivable of $270,000, an increase in inventory of $264,000, an increase in contract assets
of $284,000, and a decrease in accounts payable and other accrued liabilities of $111,000.
Cash Flows from Investing Activities
For the nine months
ended March 31, 2023, cash used in investing activities was $1,275,000. Cash used in investing activities consisted of $1,221,000
primarily related to our enterprise resource planning infrastructure investments and $54,000 in expenditures for intangible asset
costs.
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Cash Flows from Financing Activities
For the nine months ended
March 31, 2023, cash used in financing activities was $418,000. Cash used in financing activities consisted primarily of $305,000
for taxes paid on net share settlement of stock option exercises and $153,000 used for our share repurchase program partially offset
by cash received for stock option exercises.
Adequacy of Capital Resources
Our primary working capital
requirements relate to adding employees to our sales force and support functions, continuing infrastructure investments, and supporting
general corporate needs, including financing equipment purchases and other capital expenditures incurred in the ordinary course
of business. Based on our current operational performance, we believe our working capital of $28,752,000 and available borrowings
under our existing credit facility will provide adequate liquidity during fiscal 2023.
Our credit facility provides
us with a revolving line of credit. Interest on borrowings on the line of credit accrues at the prime rate (8.0% at March 31, 2023)
less 1.00% and is payable monthly. There was no outstanding principal balance on the line of credit as of March 31, 2023 or June
30, 2022. The amount eligible for borrowing on the line of credit is limited to the lesser of $2,500,000 or 57.00% of eligible
accounts receivable, and the line of credit expires on December 18, 2023, if not renewed. As of March 31, 2023, the maximum $2,500,000
was available under the line of credit. Payment obligations under the line of credit are secured by a security interest in substantially
all of our tangible and intangible assets.
The documents governing
our line of credit contain certain financial and nonfinancial covenants that include a minimum tangible net worth of not less than
$10,125,000 and restrictions on our ability to incur certain additional indebtedness or pay dividends.
Any failure to comply with
these covenants in the future may result in an event of default, which if not cured or waived, could result in the lender accelerating
the maturity of our indebtedness, preventing access to additional funds under the line of credit, requiring prepayment of outstanding
indebtedness, or refusing to renew the line of credit. If the maturity of the indebtedness is accelerated or the line of credit
is not renewed, sufficient cash resources to satisfy the debt obligations may not be available and we may not be able to continue
operations as planned. If we are unable to repay such indebtedness, the lender could foreclose on these assets.
For the nine months ended March
31, 2023 and 2022, we spent $1,221,000 and $980,000, respectively, on property and equipment. We currently expect to finance planned
equipment purchases with cash flows from operations or borrowings under our credit facility. We may need to incur additional debt
if we have an unforeseen need for additional capital equipment or if our operating performance does not generate adequate cash
flows.
While the impact of macro-economic
factors such as inflation are difficult to predict, we believe our cash, cash equivalents and cash flows from operations will be
sufficient to meet our working capital, capital expenditure, operational cash requirements for fiscal 2023 and the foreseeable
future. We will continue to evaluate our projected expenditures relative to our available cash and evaluate financing alternatives
in order to satisfy our working capital and other cash requirements.
Information Regarding Forward-Looking Statements
Statements contained in
this Quarterly Report on Form 10-Q that are not statements of historical fact should be considered forward-looking statements within
the meaning of the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities
Exchange Act of 1934, as amended (the “Exchange Act”). Forward- looking statements include, but are not limited to,
statements regarding: the expected impact of the COVID-19 pandemic on our business; our business strategy, including our intended
level of investment in R&D and marketing activities; our expectations with respect to earnings, gross margins and sales growth,
industry relationships, marketing strategies and international sales; estimated sizes of markets into which our products are or
may be sold; our business strengths and competitive advantages; our ability to grow additional sales distribution channels; our
intent to retain any earnings for use in operations rather than paying dividends; our expectation that our products will continue
to qualify for reimbursement and payment under government and private insurance programs; our intellectual property plans and practices;
the expected impact of applicable regulations on our business; our beliefs about our manufacturing processes; our expectations
and beliefs with respect to our employees and our relationships with them; our belief that our current facilities are adequate
to support our growth plans; our expectations with respect to ongoing compliance with the terms of our credit facility; our expectations
regarding the ongoing availability of credit and our ability to renew our line of credit; enhancements to our products and services;
expected excise tax exemption for the SmartVest System; and our anticipated revenues, expenses, capital requirements and liquidity.
Words such as “anticipate,” “believe,” “continue,” “could,” “estimate,”
“expect,” “intend,” “may,” “ongoing,” “plan,” “potential,”
“project,” “goal,” “target,” “should,” “will,” “would,”
and similar expressions, including the negative of these terms, are intended to identify forward-looking statements but are not
the exclusive means of identifying such statements. Although we believe these forward-looking statements are reasonable, they involve
risks and uncertainties that may cause actual results to differ materially from those projected by such statements. Such statements
involve known and unknown risks, uncertainties and other factors that may cause our actual results or our industry’s actual
results, levels of activity, performance or achievements to be materially different from the information expressed or implied by
the forward-looking statements.
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Factors that could cause
actual results to differ from those discussed in the forward-looking statements include, but are not limited to, the following:
● ability to obtain reimbursement from Medicare, Medicaid, or private insurance
payers for our products including the potential adverse impact of an expiration of the CMS waiver for certain respiratory diseases;
● component or raw material shortages, changes to lead times or significant
price increases;
● business disruption from the anticipated implementation of a new enterprise
resource planning software system;
● adverse changes to state and federal health care regulations;
● our ability to maintain regulatory compliance and to gain future regulatory
approvals and clearances;
● entry of new competitors including new drug or pharmaceutical discoveries;
● adverse economic and business conditions or intense competition;
● the risks associated with our planned
sales force expansion;
● wage and component price inflation;
● technical problems with our research and products;
● the duration, extent and severity of the COVID-19 pandemic, including its
effects on our business, operations and employees as well as its impact on our customers and distribution channels and on economies
and markets more generally;
● the risks associated with cyberattacks, data breaches, computer viruses
and other similar security threats;
● changes affecting the medical device industry;
● our ability to develop new sales channels
for our products such as the home care distributor channel;
● adverse international health care regulation impacting current international
business;
● our ability to renew our line of credit
or obtain additional credit as necessary; and
● our ability to protect and expand our intellectual property portfolio.
This list of factors is
not exhaustive, however, and these or other factors, many of which are outside of our control, could have a material adverse effect
on us and our results of operations. Therefore, you should consider these risk factors with caution and form your own critical
and independent conclusions about the likely effect of these risk factors on our future performance. Forward-looking statements
speak only as of the date on which the statements are made, and we undertake no obligation, and expressly disclaim any such obligation,
to update any forward-looking statement for any reason other than as required by law, even if new information becomes available
or other events occur in the future. You should carefully review the disclosures and the risk factors described in this and other
documents we file from time to time with the Securities and Exchange Commission (the “SEC”), including our Annual Report
on Form 10-K for fiscal 2022. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified
in their entirety by the cautionary statements set forth herein.
Item 3. Quantitative and Qualitative Disclosures About Market Risk.
As a smaller reporting company, we are not required
to provide disclosure pursuant to this Item.
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Text extracted from the filing as submitted to EDGAR. Formatting, tables and exhibits are simplified for reading; the original document is authoritative for anything you rely on.