MINERAL WELLS, Texas--(BUSINESS WIRE)--Alpha-Stim, cranial electrotherapy stimulation (CES) devices providing treatment for anxiety, depression, insomnia and pain, announces its user-supported campaign to change an FDA rule regarding Pre-Market Approval (PMA), the medical device equivalent of a new drug application. FDA is proposing a rule that would now require PMA for CES, while for the past 30 years CES devices have been legally cleared to market in the USA by FDA.

Approved for over the counter sales in Europe, China and Canada, the Alpha-Stim devices have gone through an extensive review process for the FDA six times since 1981 and have been cleared to market. Alpha-Stim is highly respected in the medical industry (doctors, psychologists, addiction professionals, etc.) and military communities, resulting, to date, in over 100 written objections to this proposed rule on behalf of Alpha-Stim, indicating its safety, lack of side effects, and above all, its effectiveness.

Texas Congressman Joe Barton has recently submitted the following statement to the Congressional Subcommittee on Oversight and Investigations: "The Medical Device Review Process at the Food and Drug Administration (FDA) has become overly burdensome, unpredictable and inconsistent under its current leadership…Small companies and entrepreneurs want to create businesses and design products that will help save lives and be profitable."

In its comments to the proposed rule submitted to FDA docket No. FDA-2011-N-0504-0078 on October 12, 2011, Alpha-Stim has focused on three main areas of concern in the proposed rule:

  1. FDAs review of the science
  2. FDAs review of safety data
  3. FDAs evaluation of the economic impact of this ruling

EPI inc., Alpha-Stims parent company, is asking for the "valid scientific evidence" provided to FDA for CES be reviewed thoroughly and fairly. EPI asks that FDA review all of the safety data provided and revise the findings within the proposed rule. EPI has provided the FDA with valid scientific evidence showing:

  1. 99.9% of actual Alpha-Stim users considered the device effective.
  2. Only 11 out of over 50,000 Alpha-Stim users (less than 0.02%) reported adverse effects from using Alpha-Stim.
  3. 49 completed studies and 12 on-going studies conducted on Alpha-Stim support the safety and effectiveness of the device.

The economic impact of the ruling is to impose a process that the FDA estimates will cost the company $1 million, for a product they approved over 30 years ago. Alpha-Stim and its supporters find the ruling overly aggressive and in complete opposition to all the positive information found in studies that Alpha-Stim diligently provided.

Through the use of its proprietary waveform, Alpha-Stim technology applies a mild electrical current via electrodes that clip onto the earlobes. The waveform works effectively in a safe and controlled manner to gently coax the brains electrical signals to normalize. The result is safe and effective treatment of anxiety, depression, insomnia, and pain. Alpha-Stim works with the body instead of against it, and is non-invasive and gentle as compared to the strong electrical signals from other devices used in both physical medicine and psychiatry. The devices also operate without the side effects that are common to prescription medications.

To view the FDA docket including proposed rule and letters of support for Alpha-Stim, please visit and search using the proposed rules docket number: FDA-2011-N-0504.

About Alpha-Stim

Alpha-Stim is an industry leader in cranial electrotherapy stimulation (CES) devices, providing treatment for anxiety, depression, insomnia and pain, without the side effects common to prescription medications. Alpha-Stim works by applying a mild electrical current that works effectively in a safe and controlled manner. Created by experienced medical industry leaders Dr. Daniel Kirsch and the company he founded EPI inc., Alpha-Stim utilizes technology based on more research than any other therapeutic device on the market. For more information on Alpha-Stim, please visit