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U.S. FDA Medical Device Tweezer-Type Epilator Requirements

FDA Medical Device Definition: The tweezer-type epilator is an electrical device intended to remove hair. The energy provided at the tip of the tweezer used to remove hair may be radio frequency, galvanic (direct current), or a combination of radio frequency and galvanic energy.

Registrar Corp assists Tweezer-Type Epilator companies with:

  • FDA Tweezer-Type Epilator Establishment Registration
  • FDA Tweezer-Type Epilator Listing
  • FDA Tweezer-Type Epilator Label Requirements and Exceptions
  • FDA Tweezer-Type Epilator Import Information
  • FDA Tweezer-Type Epilator Detentions (Tweezer-Type Epilator Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Tweezer-Type Epilator Manufacturers (Tweezer-Type Epilator Suppliers)
       - Tweezer-Type Epilator Distributors
       - Tweezer-Type Epilator Processors
       - Tweezer-Type Epilator Repackers
       - Tweezer-Type Epilator Relabelers
       - Tweezer-Type Epilator Exporters
       - Tweezer-Type Epilator Importers
For more information about Tweezer-Type Epilator Medical Devices, simply click below:

U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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