FDA ClearanceThe Fisher Wallace Stimulator®, previously branded the Liss Cranial Stimulator®, was cleared by the FDA in 1990 for the treatment of depression, anxiety, insomnia and chronic pain - the longest tenure of regulation of any wearable neurostimulation device on the market.
The safety and effectiveness of the Fisher Wallace Stimulator® has been proven in multiple published studies, including a clinical trial conducted at Mount Sinai Hospital and published in the Journal of Nervous and Mental Disease in 2015. The device is also used by top substance abuse clinics such as Phoenix House where it increased patient retention by 50% in a 392-subject study conducted in 2012.
European and Canadian ApprovalThe Fisher Wallace Stimulator® was approved by Health Canada and the European Union's ISO/CE regulators in 2014, where it is available for sale over-the-counter (OTC).
to Use the Device
Answer a few simple questions on purchase-authorization.com.
This process takes less than 60 seconds.
Go to purchase-authorization.com to obtain same-day authorization, or have your provider fax or email a prescription or completed authorization form to Fisher Wallace. The FDA requires authorization for US patients.