Modular Medical (MODD) risk factors, FY2026 10-K

Modular Medical's FY2026 10-K, filed Jun 29, 2026, lists 46 risk factors in 2 groups. Against the prior year's 43: 3 new, 7 substantially reworded.

Risk factors listed
462 groups
New this year
3vs 43 last year
Dropped
0since the prior 10-K
Substantially reworded
7of those kept
Section length
15k wordsItem 1A

What the changes say

  • Pivot began commercial shipments in June 2026, but Modular Medical has limited operating and commercial history.
  • Net loss increased to $28.2 million in fiscal 2026 from $18.8 million, while cash fell to $6.9 million.
  • FDA clearance, manufacturing scale-up, and additional financing remain central constraints on Pivot commercialization.

What changed since the prior 10-K

New

  • NewRisks Related to Our Business, Operations and Industry

    We have a limited operating history upon which to evaluate our business and forecast our future sales and operating results and may face difficulties frequently encountered by companies in competitive and rapidly-evolving markets

    The first commercial launch of Pivot leaves limited operating history for forecasting sales and results in a competitive medical-device market.

  • NewRisks Related to Our Business, Operations and Industry

    We have a limited commercial history and limited experience marketing and selling our products. We only recently launched our commercial product, which may make it difficult to evaluate the prospects for our future viability and predict our future performance

    Limited experience marketing and selling Pivot makes future revenue, profitability, growth, and viability especially difficult to predict.

  • NewRisks Related to Our Securities

    The effective increase in the number of shares of our common stock available for issuance as a result of our reverse stock split could result in further dilution to our existing stockholders and have antitakeover implications

    Shares made available after the March 2026 reverse split could be issued by the board, diluting holders and potentially affecting takeover defenses.

Reworded

  • 49% rewrittenRisks Related to Our Business, Operations and Industry

    We are an early commercial-stage medical device company and have a history of significant operating losses; we expect to continue to incur operating losses, and we may never achieve or maintain profitability

    The reported net loss increased to $28.2 million from $18.8 million, and the focus shifted from development toward commercializing and expanding acceptance of insulin pumps.

    Was: We are a pre-revenue medical device company and have a history of significant operating losses; we expect to continue to incur operating losses, and we may never achieve or maintain profitability

  • 44% rewrittenRisks Related to Our Business, Operations and Industry

    We may not be able to utilize a significant portion of our net operating losses and tax credits

    Federal and state NOLs increased to $74.6 million and $93.6 million, R&D credits rose to $3.2 million, and ownership-change limits under Sections 382 and 383 were added.

  • 38% rewrittenRisks Related to Our Business, Operations and Industry

    If the FDA requires us to go through a lengthier, more rigorous examination for our future product candidates than we had expected, product introductions or modifications could be delayed or canceled, which could adversely affect our ability to grow our business

    The displayed FDA delay examples are unchanged; the excerpt ends before any additional revisions can be identified.

  • 35% rewrittenRisks Related to Our Business, Operations and Industry

    We might not be able to continue as a going concern

    Cash declined to $6.9 million and accumulated deficit increased to $113.0 million; an April 2026 offering added approximately $3.0 million, but funding remains insufficient for twelve months.

  • 32% rewrittenRisks Related to Our Business, Operations and Industry

    We are subject to extensive regulation by the FDA, which could restrict the sales and marketing of our insulin pump products and could cause us to incur significant costs

    The risk now identifies both MODD1 and Pivot as FDA-cleared insulin pump products, replacing the prior reference to MODD1 and expected Pivot clearance.

  • 29% rewrittenRisks Related to Our Business, Operations and Industry

    We may not be able to successfully scale-up manufacturing of our products in sufficient quality and quantity, which would delay or prevent us from commercializing our products

    Manufacturing scale-up now centers on Pivot rather than MODD1, reflecting the company’s commercial product transition.

  • 26% rewrittenRisks Related to Our Business, Operations and Industry

    We may not receive the necessary regulatory clearance or approvals for our insulin pump products, and failure to timely obtain necessary clearances and/or approvals could harm our then operations, including our ability to commercialize our products

    The text now refers to insulin pump products in the plural; the provided passage shows no substantive change to the 510(k) clearance risk.

All 46 risk factors

Headings as the filing states them, in filing order.

Risks Related to Our Business, Operations and Industry

  1. 01We might not be able to continue as a going concern35% rewritten
  2. 02We are an early commercial-stage medical device company and have a history of significant operating losses; we expect to continue to incur operating losses, and we may never achieve or maintain profitability49% rewritten
  3. 03We will need substantial additional funding to complete subsequent phases of the development of our insulin pump products and to operate our business and such funding may not be available or, if it is available, such financing is likely to substantially dilute our existing stockholders
  4. 04We have a limited operating history and historical financial information upon which you may evaluate our performance
  5. 05The amount of financing we require will depend on a number of factors, many of which are beyond our control. Our results of operations, financial condition and stock price are likely to be adversely affected if our funding requirements increase or are otherwise greater than we expect
  6. 06Our future cash requirements may differ significantly from our current estimates
  7. 07We may not be able to utilize a significant portion of our net operating losses and tax credits44% rewritten
  8. 08Technological breakthroughs in diabetes monitoring, treatment or prevention could render our insulin pump products obsolete
  9. 09Any failure to attract and retain skilled directors, executives, employees and consultants could impair our product development and commercialization activities
  10. 10Our operations are substantially dependent upon key personnel
  11. 11We may not be able to identify, negotiate and maintain the strategic alliances necessary to develop and commercialize our products and technologies, and we will be dependent on our corporate partners if we do
  12. 12We may not receive the necessary regulatory clearance or approvals for our insulin pump products, and failure to timely obtain necessary clearances and/or approvals could harm our then operations, including our ability to commercialize our products26% rewritten
  13. 13If the FDA requires us to go through a lengthier, more rigorous examination for our future product candidates than we had expected, product introductions or modifications could be delayed or canceled, which could adversely affect our ability to grow our business38% rewritten
  14. 14We have a limited operating history upon which to evaluate our business and forecast our future sales and operating results and may face difficulties frequently encountered by companies in competitive and rapidly-evolving marketsNew
  15. 15We have a limited commercial history and limited experience marketing and selling our products. We only recently launched our commercial product, which may make it difficult to evaluate the prospects for our future viability and predict our future performanceNew
  16. 16Our competitors may develop products that are more effective, safer and less expensive than ours
  17. 17We expect to rely on third-party manufacturers and will be dependent on their quality and effectiveness
  18. 18We may not be able to successfully scale-up manufacturing of our products in sufficient quality and quantity, which would delay or prevent us from commercializing our products29% rewritten
  19. 19We are dependent upon third-party suppliers to manufacture our product, and this makes us vulnerable to supply shortages and price increases; we may not be able to obtain an adequate supply of components on a timely basis or at all
  20. 20We may be subject to potential product liability and other claims that could materially impact our business and financial condition
  21. 21Legislative, regulatory, or medical cost reimbursement changes may adversely impact our business
  22. 22We are subject to extensive regulation by the FDA, which could restrict the sales and marketing of our insulin pump products and could cause us to incur significant costs32% rewritten
  23. 23Medical devices may be marketed only for the indications for which they are approved or cleared. Further, 510(k) clearance can be revoked if safety or effectiveness problems develop once the device is on the market
  24. 24The occurrence of any of these events would have a material adverse effect on our business, financial condition and results of operations and could result in stockholders losing their entire investment
  25. 25Our success depends substantially upon our ability to obtain and maintain intellectual property protection relating to our insulin pump products and research technologies
  26. 26If we are sued for infringing on third-party intellectual property rights, it will be costly and time-consuming, and an unfavorable outcome would have a significant adverse effect on our business
  27. 27If we are unable to protect the confidentiality of our proprietary information, the value of our technology and products could be adversely affected
  28. 28Intellectual property rights do not necessarily address all potential threats to our competitive advantage
  29. 29Healthcare reform and drug-pricing reform laws could adversely affect our products and financial condition
  30. 30We may bring infringement claims or other legal proceedings against third parties, causing us to spend substantial resources on litigation and exposing our own intellectual property portfolio to challenge
  31. 31We may become involved in disputes with our present or future contract partners over intellectual property ownership or other matters, which would have a significant effect on our business
  32. 32Our insulin pump products may be subject to recalls, which would harm our reputation, business operations and financial results

Risks Related to Our Securities

  1. 33Any disruption and/or instability in economic conditions and capital markets could adversely affect our ability to access the capital markets, and thus adversely affect our business and liquidity
  2. 34International trade policies, including protectionist trade policies, such as tariffs and sanctions, could adversely affect our business, results of operations and financial condition
  3. 35Ongoing uncertainty regarding trade policies may also complicate our short- and long-term strategic planning, and that of our partners and customers, including decisions regarding hiring, product strategy, capital investment, supply chain design and geographic expansion
  4. 36Third parties might attempt to gain unauthorized access to our network or seek to compromise our products
  5. 37We are subject to oversight by the SEC and other regulatory agencies. Investigations by those agencies could divert management’s focus and could have a material adverse effect on our reputation and financial condition
  6. 38If we are unable to satisfy the continued listing requirements of Nasdaq, our common stock could be delisted and the price and liquidity of our common stock may be adversely affected
  7. 39We are a “smaller reporting company” and, as a result of the reduced disclosure and governance requirements applicable to smaller reporting companies, our common stock may be less attractive to investors
  8. 40We do not expect any cash dividends to be paid on our shares of common stock for the foreseeable future
  9. 41If the beneficial ownership of our common stock continues to be concentrated, it may prevent our stockholders from influencing significant corporate decisions
  10. 42Future sales of our securities could adversely affect the market price of our common stock and our future capital-raising activities could involve the issuance of equity securities, which would dilute your investment and could result in a decline in the trading price of our common stock
  11. 43The effective increase in the number of shares of our common stock available for issuance as a result of our reverse stock split could result in further dilution to our existing stockholders and have antitakeover implicationsNew
  12. 44Our articles of incorporation allow for our board of directors to create new series of preferred stock without further approval by our stockholders, which could adversely affect the rights of the holders of our common stock
  13. 45Sustained inflation could have a material adverse effect on our business, financial condition, results of operations and liquidity
  14. 46Our board of directors is able to adopt recapitalizations through forward or reverse splits of our outstanding shares of common stock without stockholder approval

Other Modular Medical 10-Ks

  • FY2025 10-K risk factors
    43 risks

    Pre-revenue medical device company with $13.1M cash and $84.8M accumulated deficit raising going concern doubts.

    Filed Jun 20, 2025

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.