Odyssey Health, Inc. (ODYY)
Business Summary
Odyssey Health, Inc. operates in the medical device and pharmaceutical development industry, with a corporate mission to create or acquire distinct assets, intellectual property, and technologies with an emphasis on acquisition targets that have superior clinical utility and serve an unmet medical need. The company's business model is to develop or acquire medical-related products, engage third parties to help develop such products, complete clinical trials, and manufacture products according to U.S. Food and Drug Administration regulations. The company operates in one reportable segment, which includes all of its business activities. The company has two different technologies it plans to develop: the CardioMap heart monitoring and screening device and the Save-A-Life choking rescue device. The company is not currently selling or marketing any products, as its products need development, and FDA clearance or approval to market its products will be required to sell in the United States. In addition, the company would require additional European Union or country specific clearance or approvals to sell internationally. The company has no products authorized for commercial distribution in the United States, Europe or any other country. Due to funding constraints and market conditions, the Save-A-Life will be prioritized for further development, while the CardioMap development program will remain suspended in the near term.
The primary competition for the company's products and services is from existing companies offering electrocardiogram equipment and anti-choking devices, as well as other pharmaceutical companies engaged in the development of orphan drugs. For the Save-A-Life choking rescue device, competitors include Dechoker, which utilizes a hand powered pump system to extract blockages and can be used for choking first aid on anyone 12 months or older; LifeVac, which is designed with a valve to prevent any air from exiting through the mask, creating a one-way suction to remove the lodged food or object; and Act+Fast Heimlich maneuver training vests, which enable students to develop confidence in their ability to perform the Abdominal Thrust Maneuver as recommended by the American Heart Association. For the CardioMap technology, none of the current rapid EKG devices have the ability to digitally map the heart, and each of the competitors give EKG read outs only. These competitors include CardioResting (Nasiff), a complete and full-featured 12 lead PC based cardiology system that is electronic medical record compatible with an unlimited database; Welch Allyn PC Based Electrocardiograph, which automatically transfers patient information and test data into most EMRs; and QardioCore, a wireless medical grade ambulatory EKG monitoring system that can identify atrial fibrillation and other arrhythmias without wires, gels or patches and is 100% deployed remotely. The company believes that its CardioMap technology, if FDA cleared or approved, could provide a better level of diagnosis with its improved sensitivity levels that can detect early warning signs that would normally be invisible with standard EKG devices, and could dramatically cut the costs associated with the detection of ischemic heart disease.
The company generates no revenue and has not generated any revenue or profit from operations since its inception. The company's business model is to develop or acquire medical-related products, engage third parties to help develop such products, complete clinical trials, and manufacture products according to FDA regulations. The company intends to acquire other technologies and assets and plans to be a trans-disciplinary product development company involved in the discovery, development and commercialization of products and technologies that may be applied over various medical markets. The company plans to license, improve and/or develop its products and identify and select distribution channels. The company intends to establish agreements with distributors to get products to market quickly as well as to undertake and engage in its own direct marketing efforts. The company will determine the most effective method of distribution for each unique product that it includes in its portfolio. The company will engage third-party research and development firms who specialize in the creation of its products to assist it in the development of its own products, and it will apply for trademarks and patents once it has developed proprietary products. If the FDA clears or approves the company's product candidates to be marketed commercially, the company intends to enter into agreements with industry partners or qualified distributors throughout the United States, and a similar approach will be pursued if its product candidates are cleared or approved for marketing outside of the United States. The company intends to require such partners or distributors to pay it an initial license fee, as well as royalties based on gross sales, with exclusivity retained based on a mutually agreeable semi-annual or quarterly sales minimum. The company has also decided to focus on international growth because, generally, such international license agreements provide a stronger path to revenue and earnings than purely domestic products.
The CardioMap System is intended to be a heart monitoring and screening device based on a novel method of Dispersion Mapping in electrocardiogram analysis for the early, non-invasive testing for coronary heart disease. The heart monitoring system is intended to provide high quality 3-D visualization and diagnosis of the heart using advanced signal analysis. The product is being designed for use in a professional setting or in remote settings including in-home use. The company has exclusive, royalty free rights to United States patent number 7,519,416 B2 related to the CardioMap technology. CardioMap was developed by VE Science Technology LLC, from whom the company purchased the product rights. The company has a working model of the device and associated software and plans to further develop the technology for clinical trials and a 510K FDA submission when funding is secured. To sell, market and distribute the CardioMap product, clearance or approval from the FDA is required, and such clearance or approval has not been obtained at this time. The product development plan for CardioMap shows concept, engineering model, and prototype as complete, with clinical trial and FDA submission as TBD. This project is not currently being funded.
The Save-A-Life choking rescue device was acquired in July 2019 when the company purchased all intellectual property including two patents for the choking rescue device: patent Number RE45,535 E, and patent Number 8,454,624 B2. The Save-A-Life device is currently in development and is designed to be a safe, and easy-to-use device for removing a lodged mass from the throat of a choking victim. The device includes a pump for creating a vacuum chamber, which is connected seamlessly with a replaceable/disposable mouthpiece. In an emergency, the SAL may be easily inserted into the victim's mouth, which depresses the tongue providing a clear application. By pressing an activation button on the device, the internal pump is intended to deliver the appropriate amount of instantaneous vacuum to dislodge the mass without harm or damage to the person. The application is intended to be instantly effective as the device will be operational and effective in a matter of seconds. To sell, market and distribute the Save-A-Life product, clearance or approval from the FDA is required, and FDA clearance or approval has not been obtained at this time. The product development plan for the Save-A-Life shows concept, engineering model, and prototype as complete, with clinical trial and FDA submission as TBD. This project is not currently being funded.
During the fiscal year ended July 31, 2026, the company entered into several significant financing and operational developments. On October 23, 2026, the company entered into a Global Amendment with Mast Hill Fund, L.P. covering all four of its promissory notes held by Mast Hill, including each tranche funded under the Master Note. Under the Global Amendment, the maturity date of each of the notes was extended to January 31, 2027; Mast Hill agreed to a one-time waiver of any event of default under Section 3.1 or Section 3.2 of the notes that occurred on or before October 23, 2026, which includes the company's nonpayment of the August 2025 note at maturity and its failure to maintain the Reserved Amount; and Mast Hill agreed to a one-time waiver of any event of default under Section 3.2 of the notes that may occur from October 23, 2026 through January 31, 2027 as a result of the company's failure to satisfy the Reserved Amount. The company also transitioned its common stock from the OTCQB to the OTCID Basic Market effective October 1, 2026, after receiving notice on July 21, 2026 from OTC Markets Group that its common stock was not in compliance with the OTCQB minimum closing bid price requirement of $0.01 per share, and paid a fee of $8,040 to OTC Markets Group for the transition. As of October 27, 2026, the company had 110,218,663 shares of common stock outstanding and 500,000,000 shares authorized.
For the fiscal year ended July 31, 2026, the company's net loss allocable to common stockholders was $5,729,693, and it had an accumulated deficit of $68,475,530 at July 31, 2026. As of July 31, 2026, the company had current liabilities of $12,277,546, current assets of $147,859, and a working capital deficit of $12,129,687. As of July 31, 2026, the company had $4,876,282 in aggregate principal amount of convertible notes outstanding, plus accrued interest, of which $3,835,282 was owed to Mast Hill Fund, L.P. The company has not generated any revenue or profit from operations since its inception. Based on its average monthly expenses and current burn rate, the company estimates that its cash on hand will not be sufficient to support its operations through the balance of this calendar year. The company's independent registered public accounting firm has issued its audit opinion on the company's consolidated financial statements for the fiscal year ended July 31, 2026, including an explanatory paragraph as to substantial doubt with respect to the company's ability to continue as a going concern.
Business Outlook & Financial Sufficiency
The company's growth strategy is focused on several areas. First, once any of its products in development are approved by the appropriate regulatory agency, the company will enter into distribution agreements with companies who have sales professionals with experience selling through a variety of sales methods, which will allow it to achieve sales and revenue more quickly in the medical products industries. Second, when funding allows, the company intends to pursue development of CardioMap technology for use in other areas of the human body, such as the brain, liver and kidney. Third, the company intends to pursue the development and acquisition of other product candidates and market any new products, if cleared or approved by regulatory bodies, as capital resources permit. Fourth, the company intends to seek partners to assist with the further development and clinical trials of its technologies, with partnerships potentially in the form of government grants or from industry medical companies. The company has also decided to focus on international growth because, generally, such international license agreements provide a stronger path to revenue and earnings than purely domestic products. The company's objective is to eventually grow revenue through marketing and sales of each of its product candidates, CardioMap and Save-A-Life.
The company's product development plans for both CardioMap and Save-A-Life show concept, engineering model, and prototype as complete, with clinical trial and FDA submission as TBD. These product development plans are estimates only and are subject to change based on the company's ability to fund the programs, technical risks, the clinical pathway and regulatory approvals. Both projects are not currently being funded. Due to funding constraints and market conditions, the Save-A-Life will be prioritized for further development, while the CardioMap development program will remain suspended in the near term. The company has a working model of the CardioMap device and associated software and plans to further develop the technology for clinical trials and a 510K FDA submission when funding is secured. To sell, market and distribute the CardioMap and Save-A-Life products, clearance or approval from the FDA is required, and such clearance or approval has not been obtained at this time.
The company expects to incur significant ongoing costs and obligations related to its investment in infrastructure and growth and for regulatory compliance, which could have a material adverse impact on its results of operations, financial condition and cash flows. The company expects its expenses to increase over time in connection with its ongoing activities, particularly if and as it invests in marketing and distribution capabilities in support of developing and potentially commercializing its products in the U.S., if cleared or approved; makes improvements to product design; conducts clinical or other trials of the products, subject to discussion with the FDA; pursues regulatory clearances and approvals; maintains, expands and protects its intellectual property portfolio; engages third party manufacturers; and adds additional personnel. Increased operating costs may cause the amount of financing that the company requires to increase. The company's efforts to grow its business may be costlier than it expects, and it may not be able to increase its revenue enough to offset its higher operating expenses.
The company's operational outlook is constrained by its limited financial resources. The company has two employees and does not intend to hire additional employees in the foreseeable future. The company engages people who provide services to it as part-time consultants, each of whom may devote part of their working time to other business endeavors, including consulting relationships with other corporate entities, and may have responsibilities to these other entities. The company's success is dependent upon the ability, expertise and judgment of its senior management, and it currently has a very small management team. The company has not obtained key person life insurance on any of its key employees. The company's future success depends significantly on the skills and efforts of Joseph Michael Redmond, President, CEO and Director and other key personnel.
The company's capital allocation priorities are focused on raising additional capital to fund its operations and product development. The company requires additional debt or equity financing to implement its business plan and marketing strategy. The company has financed its operations in the past by issuing secured and unsecured convertible debt and equity securities in private placements, in some cases with equity incentives for the investor in the form of warrants to purchase its common stock, and it has borrowed from related parties. The company has sought, and will continue to seek, various sources of financing. External financing, predominantly by the issuance of equity and debt, will be sought to finance the company's operations; however, there can be no certainty that such funds will be available at terms acceptable to the company. The company currently has no commitments for additional financing, and it has not identified any source of the capital required for its ongoing operations. The company does not expect to be able to raise any additional capital through debt financing from traditional lending sources since it is not currently generating a profit from operations, and therefore it only expects to raise money through equity financing via the sale of its common stock or equity-linked securities such as convertible debt.
The company faces significant headwinds and constraints that management has explicitly flagged. The company is in the development stage and is currently seeking additional capital, mergers, acquisitions, joint ventures, partnerships and other business arrangements to expand its product offerings and generate revenue. The company's ability to continue as a going concern is dependent upon its future ability to generate revenue and achieve profitable operations and, in the meantime, to obtain the necessary financing to meet its obligations and repay its liabilities when they become due. Based on the company's average monthly expenses and current burn rate, it estimates that its cash on hand will not be sufficient to support its operations through the balance of this calendar year. The company has substantial convertible note obligations maturing on January 31, 2027 that it does not have the funds to repay, and the waivers it has received from its principal noteholder are limited. The company does not currently have sufficient funds to repay the Mast Hill notes at January 31, 2027, and unless it obtains additional financing, further extends the maturity date, increases its authorized shares, or otherwise restructures these obligations before that date, it expects to be in default. Upon an event of default that is not waived, the company's noteholders may declare all amounts immediately due and payable, apply default interest and increased default amounts (which, under certain of the Mast Hill notes, include a default amount equal to 150% of outstanding principal and accrued interest and default interest at 16% per annum), terminate the Maintenance Agreement, and pursue collection and other remedies available under the notes and related agreements. If the company's noteholders accelerate its indebtedness or enforce their rights, the company may be forced to seek protection under the U.S. Bankruptcy Code, and its stockholders could lose their entire investment.
The company's common stock no longer trades on the OTCQB and is now quoted on the OTCID Basic Market, which may reduce liquidity and adversely affect its stock price. Until September 30, 2026, the company's common stock was quoted on the OTCQB. On July 21, 2026, the company received notice from OTC Markets Group that its common stock was not in compliance with the OTCQB minimum closing bid price requirement of $0.01 per share. To remain eligible for quotation on the OTCQB, the company's closing bid price needed to be $0.01 or higher for ten consecutive trading days by October 19, 2026. Because the company did not expect to regain compliance by that date, it paid a fee of $8,040 to OTC Markets Group and transitioned its common stock to the OTCID Basic Market effective October 1, 2026. The OTCID Basic Market is a lower market tier than the OTCQB. Quotation on the OTCID may reduce liquidity in the company's common stock, cause some broker-dealers to restrict or decline trading in it, limit the company's ability to raise capital, and adversely affect its stock price. To remain on the OTCID, the company must continue to satisfy its eligibility requirements, including remaining current in its public disclosure. If it fails to do so, its common stock may be moved to the Pink Limited market or to the Expert Market, where quotations are not publicly available and investors may be unable to sell their shares. In addition, if the company fails to remain current in its SEC periodic reports, the SEC could revoke the registration of its common stock under Section 12(j) of the Exchange Act.
Management Sentiments & Priorities
Management's message to shareholders emphasizes the company's development-stage status and its critical need for additional capital. The company's corporate mission is to create or acquire distinct assets, intellectual property, and technologies with an emphasis on acquisition targets that have superior clinical utility and serve an unmet medical need. Management has stated that the company's ability to continue as a going concern is dependent upon its future ability to generate revenue and achieve profitable operations and, in the meantime, to obtain the necessary financing to meet its obligations and repay its liabilities when they become due. Based on the company's average monthly expenses and current burn rate, management estimates that its cash on hand will not be sufficient to support its operations through the balance of this calendar year. The company has not generated any revenue or profit from operations since its inception. Management's strategic priorities for the period ahead are to prioritize the Save-A-Life choking rescue device for further development while suspending the CardioMap development program in the near term due to funding constraints and market conditions; to seek additional capital through equity financing via the sale of common stock or equity-linked securities such as convertible debt; and to pursue the development and acquisition of other product candidates and market any new products, if cleared or approved by regulatory bodies, as capital resources permit. Management has also stated that the company intends to seek partners to assist with the further development and clinical trials of its technologies, with partnerships potentially in the form of government grants or from industry medical companies.
Financial Details
For the fiscal year ended July 31, 2026, the company reported a net loss allocable to common stockholders of $5,729,693, compared to a net loss allocable to common stockholders of $5,729,693 for the fiscal year ended July 31, 2025. The company has not generated any revenue or profit from operations since its inception, and total revenue was $0 for both fiscal years. The company had an accumulated deficit of $68,475,530 at July 31, 2026. As of July 31, 2026, the company had current liabilities of $12,277,546, current assets of $147,859, and a working capital deficit of $12,129,687. As of July 31, 2026, the company had $4,876,282 in aggregate principal amount of convertible notes outstanding, plus accrued interest, of which $3,835,282 was owed to Mast Hill Fund, L.P. The company's independent registered public accounting firm has issued its audit opinion on the company's consolidated financial statements for the fiscal year ended July 31, 2026, including an explanatory paragraph as to substantial doubt with respect to the company's ability to continue as a going concern. The company operates in one reportable segment, which includes all of its business activities.
Risk Factors
The company faces substantial doubt about its ability to continue as a going concern. For the fiscal year ended July 31, 2026, the company's net loss allocable to common stockholders was $5,729,693, and it had an accumulated deficit of $68,475,530 at July 31, 2026. As of July 31, 2026, the company had current liabilities of $12,277,546, current assets of $147,859, and a working capital deficit of $12,129,687. Based on its average monthly expenses and current burn rate, the company estimates that its cash on hand will not be sufficient to support its operations through the balance of this calendar year. The company has substantial convertible note obligations maturing on January 31, 2027 that it does not have the funds to repay. As of July 31, 2026, the company had $4,876,282 in aggregate principal amount of convertible notes outstanding, plus accrued interest, of which $3,835,282 was owed to Mast Hill Fund, L.P. The company does not currently have sufficient funds to repay the Mast Hill notes at January 31, 2027, and unless it obtains additional financing, further extends the maturity date, increases its authorized shares, or otherwise restructures these obligations before that date, it expects to be in default. Upon an event of default that is not waived, the company's noteholders may declare all amounts immediately due and payable, apply default interest and increased default amounts (which, under certain of the Mast Hill notes, include a default amount equal to 150% of outstanding principal and accrued interest and default interest at 16% per annum), terminate the Maintenance Agreement, and pursue collection and other remedies available under the notes and related agreements. If the company's noteholders accelerate its indebtedness or enforce their rights, the company may be forced to seek protection under the U.S. Bankruptcy Code, and its stockholders could lose their entire investment. The company's variable-price convertible notes could cause substantial dilution and a decline in its stock price, and it does not have sufficient authorized shares to satisfy all potential conversions. As of October 27, 2026, the company had 110,218,663 shares of common stock outstanding and 500,000,000 shares authorized. Based on recent trading prices, the conversion of all outstanding notes and accrued interest would require the issuance of substantially more shares of common stock than are currently authorized and available for issuance.
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- [942] Item 1, Business — General
- [943] Item 1, Business — General
- [944] Item 1, Business — General
- [945] Item 1, Business — General
- [946] Item 1, Business — General
- [947] Item 1, Business — General
- [948] Item 1, Business — General
- [949] Item 1, Business — General
- [950] Item 1, Business — General
- [951] Item 1, Business — General
- [952] Item 1, Business — General
- [953] Item 1, Business — General
- [954] Item 1, Business — General
- [955] Item 1, Business — General
- [956] Item 1, Business — General
- [957] Item 1, Business — General
- [958] Item 1, Business — General
- [959] Item 1, Business — General
- [960] Item 1, Business — General
- [961] Item 1, Business — General
- [962] Item 1, Business — General
- [963] Item 1, Business — General
- [964] Item 1, Business — General
- [965] Item 1, Business — General
- [966] Item 1, Business — General
- [967] Item 1, Business — General
- [968] Item 1, Business — General
- [969] Item 1, Business — General
- [970] Item 1, Business — General
- [971] Item 1, Business — General
- [972] Item 1, Business — General
- [973] Item 1, Business — General
- [974] Item 1, Business — General
- [975] Item 1, Business — General
- [976] Item 1, Business — General
- [977] Item 1, Business — General
- [978] Item 1, Business — General
- [979] Item 1, Business — General
- [980] Item 1, Business — General
- [981] Item 1, Business — General
- [982] Item 1, Business — General
- [983] Item 1, Business — General
- [984] Item 1, Business — General
- [985] Item 1, Business — General
- [986] Item 1, Business — General
- [987] Item 1, Business — General
- [988] Item 1, Business — General
- [989] Item 1, Business — General
- [990] Item 1, Business — General
- [991] Item 1, Business — General
- [992] Item 1, Business — General
- [993] Item 1, Business — General
- [994] Item 1, Business — General
- [995] Item 1, Business — General
- [996] Item 1, Business — General
- [997] Item 1, Business — General
- [998] Item 1, Business — General
- [999] Item 1, Business — General
- [1000] Item 1, Business — General
Analysis on 10/28/2026