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U.S. FDA Medical Device Endodontic Paper Point Requirements


FDA Medical Device Definition: An endodontic paper point is a device made of paper intended for use during endodontic therapy to dry, or apply medication to, the root canal of a tooth.

Registrar Corp assists Endodontic Paper Point companies with:

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