AEMED is an FDA Registered, validated Specification Development Company, that designs and develops state-of-the-art medical devices. The FDA cleared StimPad® is our initial entry to market with our proprietary technologies that simplify complex electronic pain relief systems and create easy-to-use alternatives to pain relief medications. Our goal is to become the largest provider of Electro and Light therapy stimulation devices in the world and the products for Drug Free Pain Relief.
We implement Good Manufacturing Practices (GMP), International Standards Organization (ISO) Processes, and Quality Systems to the development of the StimPad® TENS devices and associated technologies. The company’s designs are compliant with:
- FDA Part 21(CFR 820)
- General Standard IEC 60601-1-1
- Medical Electrical Equipment –Part 1
- General Requirements for Safety 1: Collateral Standard: Safety Requirements for Medical Systems Directive on the Restriction of the Use of Certain Hazardous Substances in Electrical and Equipment 2002/95/EC (commonly referred to as the Restriction of Hazardous Substances Directive or RoHS).
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