Electromed, Inc. annual report, FY2021

Electromed, Inc. — Fiscal 2021 Form 10-K Summary

Reporting period: Fiscal year ended June 30, 2021, compared with fiscal 2020 ended June 30, 2020. The supplied metadata references “2020 Q4,” but the filing is an annual Form 10-K for fiscal 2021.

Business Context

Electromed develops, manufactures and sells SmartVest high-frequency chest wall oscillation airway-clearance systems for patients with compromised pulmonary function. Revenue is generated primarily through a direct-to-patient and provider model, with additional institutional, home-care distributor and international sales. The company is a smaller reporting company and operates in one medical-equipment segment.

Financial Performance and Liquidity

MetricFiscal 2021Fiscal 2020Change
Net revenue$35.756 million$32.471 million+10.1%
Gross profit$27.305 million$25.200 million+8.4%
Gross margin76.4%77.6%Down 120 bps
Operating income$3.140 million$5.118 million−38.6%
Net income$2.362 million$4.161 million−43.2%
Diluted EPS$0.27$0.47−$0.20
Operating cash flow$3.077 million$4.196 million−26.7%
  • Revenue mix: Home care revenue was $32.986 million, up 12.5%; institutional revenue was $1.549 million, down 22.6%; home-care distributor revenue was $563,000, up 30.9%; and international revenue was $658,000, down 8.4%.
  • Payer mix: Home-care Medicare revenue increased to $19.044 million from $14.863 million; commercial revenue increased to $12.530 million from $11.728 million. Medicaid revenue declined to $846,000 from $1.696 million.
  • Operating expenses: SG&A increased 12.5% to approximately $22.443 million, while R&D increased 64.0% to $1.722 million, or 4.8% of revenue.
  • Cash and working capital: Cash and cash equivalents were $11.889 million at June 30, 2021, versus $10.479 million a year earlier. Working capital was approximately $27.065 million.
  • Accounts receivable: Net accounts receivable increased to $17.032 million from $12.941 million, primarily due to growth in Medicare revenue and its approximately 13-month payment cycle.
  • Debt and liquidity: No borrowings were outstanding under the revolving credit facility. The company had up to $2.5 million available, subject to borrowing-base limits, with the facility scheduled to expire on December 18, 2021 if not renewed.
  • Capital allocation: The company repurchased 104,211 shares for $1.124 million, or $10.79 per share, leaving $1.876 million available under a $3.0 million authorization. It has never paid cash dividends.

Material Changes Versus Fiscal 2020

  • Revenue growth was driven by increased referrals and approvals, a larger sales force, hybrid virtual and in-person selling, and temporary CMS Medicare waivers related to COVID-19.
  • Institutional sales remained pressured by reduced hospital purchasing activity and infection-control protocols, although quarterly institutional revenue improved during fiscal 2021.
  • Gross margin declined because of a higher warranty reserve, costs related to discontinuing new shipments of the SV2100 model, and higher raw-material and shipping costs.
  • Profitability declined despite higher revenue because of increased SG&A and R&D investments and the absence of the $913,000 CARES Act payment recognized in fiscal 2020.
  • Operating cash flow declined as the increase in accounts receivable more than offset net income and working-capital benefits from inventory and contract assets.
  • Net other expense of $12,000 included $187,000 of data-security incident costs, partially offset by $175,000 of insurance reimbursement.

Guidance, Outlook and Management Commentary

  • Fiscal 2022 priorities include expanding the sales force, increasing direct-to-consumer marketing, improving customer support, expanding physician adoption in bronchiectasis, and developing the next-generation SmartVest device.
  • Management expects R&D spending to remain within approximately 3% to 5% of revenue in fiscal 2022 and to decrease slightly as design and testing conclude.
  • The company estimates launching the next-generation device and completing the related FDA 510(k) clearance process in the first half of fiscal 2023.
  • Management believes current working capital, operating cash flow and available credit will provide adequate liquidity for fiscal 2022.
  • The company expects to improve gross margin over time through lower next-generation product costs, supplier optimization and operating leverage, although near-term margin may vary with payer and referral mix.

Risks, Contingencies and Unusual Items

  • COVID-19 continues to create uncertainty through potential effects on clinics, hospitals, patients, supply chains, reimbursement programs and broader economic activity. CMS waivers affecting Medicare respiratory-device documentation and face-to-face requirements were scheduled to expire in October 2021.
  • Component, raw-material and packaging shortages caused longer lead times during fiscal 2021, although the company reported no material customer-shipment disruption.
  • Revenue depends significantly on third-party reimbursement. Reimbursement can be reduced by payer policies, deductibles, co-payments, coverage changes, appeals and patient discontinuation of therapy.
  • The credit facility contains financial and nonfinancial covenants, including a minimum tangible net worth of $10.125 million. Failure to renew or comply with the facility could restrict liquidity and permit acceleration or foreclosure remedies.
  • In June 2021, an unauthorized third party accessed a limited number of files containing information relating to customers, employees and some contractors. The company reported no indication of misuse and stated that insurance should cover most related costs.
  • The company faces FDA, EU MDR, reimbursement, privacy, cybersecurity, intellectual-property, product-liability and healthcare fraud-and-abuse risks.
  • The warranty reserve increased to $940,000 from $740,000, primarily because of additional components included in the calculation and higher SV2100 repair costs; management reported no increase in product warranty returns.
  • The independent auditor issued an unqualified opinion. Measurement of customer revenue net of contractual and collection adjustments was identified as the critical audit matter.

Investor Verification Items

  • Verify the status and renewal terms of the revolving credit facility after its December 18, 2021 expiration date.
  • Assess the effect of CMS waiver expiration on Medicare referrals, approval rates, revenue and accounts receivable collections.
  • Track institutional demand recovery and the sustainability of home-care referral growth.
  • Evaluate execution, regulatory clearance timing, launch costs and reimbursement coverage for the next-generation SmartVest device.
  • Review warranty-reserve trends and the financial impact of discontinuing new SV2100 shipments.
  • Monitor the data-security incident, insurance recoveries, remediation costs and any regulatory or litigation developments.
  • Reconcile revenue-recognition estimates, contract assets and the growing accounts-receivable balance, particularly for Medicare and appealed claims.