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U.S. FDA Medical Device Finger Exerciser Requirements

FDA Medical Device Definition: A powered finger exerciser is a device intended for medical purposes to increase flexion and the extension range of motion of the joints of the second to the fifth fingers of the hand.

Registrar Corp assists Finger Exerciser companies with:

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