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U.S. FDA Medical Device Grooming Adaptor Requirements

FDA Medical Device Definition: A daily activity assist device is a modified adaptor or utensil (e.g., a dressing, grooming, recreational activity, transfer, eating, or homemaking aid) that is intended for medical purposes to assist a patient to perform a specific function.

Registrar Corp assists Grooming Adaptor companies with:

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