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U.S. FDA Medical Device Ring Cutter Requirements

FDA Medical Device Definition: A ring cutter is a device intended for medical purposes that is used to cut a ring on a patient's finger so that the ring can be removed. The device incorporates a guard to prevent injury to the patient's finger.

Registrar Corp assists Ring Cutter companies with:

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