What the changes say
- The company removed its going concern and net loss warnings but disclosed it has only one covering analyst.
What changed since the prior 10-K
Dropped
- DroppedRisks related to financial, operational, commercial and manufacturing matters
The auditors of our December 31,2023 financial statements expressed substantial doubt about our ability to continue as a going concern, which may hinder our ability to obtain further financing
- DroppedRisks related to financial, operational, commercial and manufacturing matters
We have incurred significant net losses since inception and anticipate that we will continue to incur net losses for the foreseeable future and may never achieve or maintain profitability
Auditors expressed substantial doubt about the company continuing as a going concern given $0.46 million cash.
Reworded
- 39% rewrittenRisks Related to Government Regulation and Our Industry
We may experience difficulties outside the US in obtaining or maintaining regulatory clearance or approval, or exemptions therefrom, or in successfully gaining third-party reimbursement or marketing our technology, even if approved or otherwise legally marketed
No substantive textual changes were made regarding international regulatory clearances for the NOCISCAN product suite.
- 34% rewrittenRisks Related to Financial, Operational, Commercial and Manufacturing Matters
If adequate reimbursement is not available for the procedures implementing our technology, or for clinicians to provide ongoing care for patients diagnosed with our technology, it could diminish our sales or affect our ability to sell our technology
Added the disclosure that the company is reimbursed by certain third-party payors in the United Kingdom.
- 34% rewrittenRisks Related to the Ownership of Our Common Stock and IPO Warrants
If securities analysts do not publish research or reports about our business or if they publish negative evaluations of our stock, the price of our stock could decline
Disclosed that the company currently has only one securities analyst publishing research on it with no guarantee of continued coverage.
- 27% rewrittenRisks Related to Government Regulation and Our Industry
Our operations and technology are subject to pervasive and continuing FDA regulatory requirements, and failure to comply with these requirements could harm our business, financial condition and results of operations
Capitalized 'De Novo' when referring to the FDA review process.
All 53 risk factors
Headings as the filing states them, in filing order.
Risks Related To Our Nasdaq Listing
- 01We may not be able to maintain compliance with the continued listing rules of the Nasdaq Capital Market and a delisting could limit the liquidity of our stock, increase its volatility and hinder our ability to raise capital
Risks Related to Financial, Operational, Commercial and Manufacturing Matters
- 02We will need additional funding, which may not be available on acceptable terms, or at all. Failure to obtain this capital when needed may force us to delay, limit or terminate our product development efforts or other operations
- 03Raising additional capital may cause dilution to our existing stockholders, restrict our operations or require us to relinquish rights to our technologies and product candidates
- 04We are highly dependent on our senior management team and key personnel, and our business could be harmed if we are unable to attract and retain personnel necessary for our success
- 05Our MR data post-processing products currently depend on compatible use with only a limited number of MR scanners that are provided only by one manufacturer of MR devices
- 06If we are not successful in enhancing awareness of our technology, driving adoption across our current target population, increasing referrals from surgeons and clinicians, and expanding the population of eligible patients, our sales, business, financial condition and results of operations will be negatively affected
- 07Our commercial success will continue to depend on attaining significant market acceptance of our technology among physicians, surgeons, patients, clinicians and imaging facilities, and increasing the number of patients diagnosed by our technology
- 08We may be unable to compete successfully with other diagnostic options for low back pain, or may be unable to continue providing value for supporting new treatments that may not need the diagnostic information our products provide
- 09Adoption of our technology depends on positive clinical data as well as clinician acceptance of the data and our products, and negative clinical data or perceptions among these clinicians would harm our sales, business, financial condition, and results of operations
- 10If adequate reimbursement is not available for the procedures implementing our technology, or for clinicians to provide ongoing care for patients diagnosed with our technology, it could diminish our sales or affect our ability to sell our technology34% rewritten
- 11If adequate reimbursement for our temporary Category III CMS Code designation for our products cannot be obtained or we are not successful in obtaining conversion to permanent Category I codes at an adequate reimbursement level, it would diminish our sales and would affect our ability to market our technology
- 12Use of our technology requires appropriate training for proper use of our products, and inadequate training may lead to negative patient outcomes, which could harm our business, financial condition, and results of operations
- 13We expect to increase the size of our organization in the future, and we may experience difficulties in managing this growth. If we are unable to manage the anticipated growth of our business, our future revenue and operating results may be harmed
- 14We may not be able to achieve or maintain satisfactory pricing and margins for our NOCISCAN disc MRS diagnostic software products and related services, which could harm our business and results of operations
- 15Our results of operations may be harmed if we are unable to accurately forecast customer demand for our technology
Risks Related to Government Regulation and Our Industry
- 16Our operations and technology are subject to pervasive and continuing FDA regulatory requirements, and failure to comply with these requirements could harm our business, financial condition and results of operations27% rewritten
- 17If we are unable to expand the labeling claims for using our technology to include additional indications, our growth potential could be harmed
- 18Our medical device products may be subject to recalls, which could divert managerial and financial resources, harm our reputation and our business
- 19We may experience difficulties outside the US in obtaining or maintaining regulatory clearance or approval, or exemptions therefrom, or in successfully gaining third-party reimbursement or marketing our technology, even if approved or otherwise legally marketed39% rewritten
- 20These and other risks associated with international operations may harm our ability to attain or maintain profitable operations internationally, which would harm our growth potential
- 21If we fail to comply with fraud and abuse and other healthcare laws and regulations in the U.S. and internationally including those relating to kickbacks and false claims for reimbursement, we could face substantial penalties and our business, financial condition and results of operations could be harmed
- 22Regulatory compliance is expensive, complex and uncertain, and a failure to comply could lead to enforcement actions against us and other negative consequences for our business
- 23A failure to comply with governmental regulatory requirements would have a negative impact upon our business
- 24If we become subject to enforcement action by governmental regulatory agencies, our business would be negatively affected
- 25If any of these events were to occur, it would have a negative impact on our business, financial condition and results of operations
- 26Healthcare reform initiatives and other administrative and legislative proposals may harm our business, financial condition, results of operations and cash flows in our key markets
- 27Our employees, independent contractors, consultants, commercial partners and vendors may engage in misconduct or other improper activities, including noncompliance with regulatory standards and requirements, which could harm our business, financial condition and results of operations
- 28We face potential liability related to the privacy of health information we obtain
Risks Related To Our Intellectual Property
- 29We may not be successful in obtaining or maintaining necessary rights to any products or processes we may have or develop through acquisitions and in-licenses
- 30Patents directing to our technology could be found invalid or unenforceable if challenged in court or before administrative bodies in the United States or abroad, which could harm our business, financial condition and results of operations
- 31Obtaining and maintaining our patent protection depends on compliance with various procedural measures, document submissions, fee payments and other requirements imposed by government patent agencies, and our patent protection could be reduced or eliminated for non-compliance with these requirements
- 32If we fail to comply with our obligations in any current or future agreements under which we license intellectual property rights from third parties or otherwise experience disruptions to our business relationships with our licensors, we could lose license rights that are important to our business
- 33If we are unable to obtain patent term extension under the Hatch-Waxman Amendments, our business may be materially harmed
- 34We have limited foreign intellectual property rights and may not be able to protect our intellectual property and proprietary rights throughout the world, which could harm our business, financial condition and results of operations
- 35Changes in U.S. patent laws, or patent laws in other countries and jurisdictions, could diminish the value of patents in general, thereby impairing our ability to protect our products
- 36We may become involved in lawsuits to protect or enforce our patents and other intellectual property rights, which could be expensive, time-consuming and unsuccessful
- 37If our trademarks and trade names are not adequately protected, then we may not be able to build name recognition in our markets of interest and our business may be harmed
- 38Intellectual property rights do not necessarily address all potential threats, and limitations in intellectual property rights could harm our business, financial condition and results of operations
- 39If we are unable to protect the confidentiality of our other proprietary information, our business and competitive position may be harmed
- 40Our inability to use software licensed from third parties, or our use of open-source software under license terms that interfere with our proprietary rights, could disrupt our business
- 41Other Risks Facing Our Company
- 42The failure of third parties to meet their contractual, regulatory and other obligations could adversely affect our business
- 43Litigation and other legal proceedings may harm our business
- 44Our operating results may fluctuate across periods, which makes our future operating results difficult to predict and could cause our operating results to fall below expectations or any guidance we may provide
- 45We will incur increased costs as a result of operating as a public company, and our management and board of directors will be required to devote substantial time to compliance with our public company responsibilities and corporate governance practices
Risks Related to the Ownership of Our Common Stock and IPO Warrants
- 46Our stock price may be volatile, and the value of our common stock and IPO Warrants may decline
- 47A significant portion of our total outstanding shares may be sold into the market, which could cause the market price of our common stock to drop significantly, even if our business is performing well
- 48The price of our common stock and IPO Warrants may be volatile and fluctuate substantially, which could result in substantial losses for investors in our common stock
- 49Because we do not expect to pay dividends in the foreseeable future, investors seeking cash dividends should not purchase shares of our common stock
- 50If securities analysts do not publish research or reports about our business or if they publish negative evaluations of our stock, the price of our stock could decline34% rewritten
- 51We are an emerging growth company and a smaller reporting company, and our compliance with the reduced reporting and disclosure requirements applicable to emerging growth companies and smaller reporting companies could make our common stock and IPO Warrants less attractive to investors
- 52We cannot predict whether investors will find our common stock less attractive as a result of our reliance on these exemptions. If some investors find our common stock less attractive, as a result, there may be a less active trading market for our common stock and our stock price may be more volatile
- 53Provisions in our corporate charter and our bylaws and under Delaware law could make an acquisition of us, which may be beneficial to our stockholders, more difficult and may prevent attempts by our stockholders to replace or remove our current management
Other Aclarion 10-Ks
- FY2024 10-K risk factors55 risks
Aclarion faces going concern doubts, Nasdaq delisting risks, and net losses totaling $6,992,927 in 2024. The business relies heavily on Siemens and Philips MR scanners and adoption of its NOCISCAN software. Growth depends on clinical data, reimbursement codes, and regulatory clearances.
Filed Apr 09, 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.