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U.S. FDA Medical Device Tongue Scraper Requirements

FDA Medical Device Definition: A manual toothbrush is a device composed of a shaft with either natural or synthetic bristles at one end intended to remove adherent plaque and food debris from the teeth to reduce tooth decay.

Registrar Corp assists Tongue Scraper companies with:

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