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U.S. FDA Medical Device Dental Stain Eraser 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 Dental Stain Eraser companies with:

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