Thank you for your interest in WhisperSom™.

We are a dedicated team of professionals and industry leaders committed to significantly improving the rates of diagnosis and treatment for millions of sleep apnea sufferers around the world through technology. Based on the data we have shared with the FDA so far, we are convinced that we have developed the medical device to do it, following FDA approval.

Sleep Apnea Market

The global sleep apnea market is approximately $4B annual with a 7.8% CAGR, and estimated to include as many as 930 million individuals with over 50 million located in the U. S. alone.

It is further estimated that 2 million sufferers are prescribed CPAP annually in North America. Of these patients, 34%, or approximately 680 thousand quit CPAP within 12 months.

Our potential customers also include the millions of sleep apnea sufferers who are still undiagnosed and those CPAP users eagerly waiting for an alternative.

Investment Case

Our financial model assumes doubling the 5% treatment rate of sleep apnea in the U.S. within 5 years while expanding internationally in select countries to generate $2 billion in net profits with 4 million patients under care.

The leading CPAP maker and the surgically implanted alternative to CPAP have approximately 5% of sleep apnea patients under care collectively with market caps of $20 billion and $5 billion respectively.

We estimate reaching profitability and our revenue goals by raising less than $30M in addition to the $5.7 million raised to date from accredited investors that include both physicians and patients.

Our stretch goal is to help raise the overall diagnosis and treatment rates to at least 50% within 5 years.

The data we have gathered in comprehensive R&D testing is convincing evidence to us that our device works as designed, and we are now raising the capital required to perform the necessary steps to rapidly bring it to market and reach profitability.

Every year in North America, close to 700,000 patients quit CPAP within the first 12 months of using it.

Most never even try it.

If you are an accredited investor as defined by Rule 501(a) of Regulation D under the 1933 Securities Act, as amended, join us in helping to develop a more effective sleep apnea solution today.

  • 1,550 Units (657 Common Voting Shares per Unit)
  • Minimum Investment:
    • Individuals – $10,000 (1 Unit)
    • Entities – $100,000 (10 Units)

To request detailed information please complete the form below:



    YesNo

    Disclaimer

    The offering is being made only by means of a private placement memorandum and subscription agreement.
    This information provided at this website shall not constitute an offer to sell or the solicitation of an offer to buy any securities nor shall there be any sale of the securities in any state in which such offer, solicitation or sale would be unlawful under the securities laws of any such state.
    The WhisperSom™ device is not commercially available at this time. It has not been cleared by the FDA and is currently undergoing development.  No representations are made as to future FDA clearance, nor as to the eventual suitability of the device with respect to any medical condition.  WhisperSom Corporation  has made an initial application to the FDA for consideration as a designated breakthrough technology for treating all forms of sleep apnea, and data from a small number of test subjects was submitted as part of that application. After reviewing the application, the FDA requested only two additional elements of information that will require further testing. That testing process is currently underway.

    Safe Harbor Statement

    This website may contain forward-looking statements regarding future events and the future performance of Whispersom Corporation. Forward-looking statements in this website include, without limitation, express or implied statements regarding: the Company’s forecasted operating results for future years; the Company’s expectations regarding its patent applications; the Company’s ability to sustain necessary liquidity; and anticipated FDA submissions. A forward-looking statement is neither a prediction nor a guarantee of future events or circumstances and is based on currently available market, operating, financial and competitive information and assumptions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those expected or projected, including, among others, risks that: the Company and its partners will not achieve the results anticipated in the statements made in this release; global economic conditions and the financial condition of the sleep apnea industry and/or adverse changes in our products could cause our results to differ from our anticipations; the Company’s dependence on a new investors makes us susceptible to changes in the timing of our plans; and the Company’s dependence on its key management personnel could leave us exposed to disruption on any termination of service. Except as required by law, the Company undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise. The Company’s guidance is based on current plans and expectations and is subject to a number of known and unknown uncertainties and risks, including those set forth under the Company’s safe harbor statement. This forecast is made as of the date of this release, and Company undertakes no obligation to update or amend this guidance whether as a result of new information, future events or otherwise.