Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Cane, Tips & Pads Regulations

U.S. FDA Medical Device Cane, Tips & Pads Requirements

FDA Medical Device Definition: Cane, crutch, and walker tips and pads are rubber (or rubber substitute) device accessories intended for medical purposes that are applied to the ground end of mobility aids to prevent skidding or that are applied to the body contact area of the device for comfort or as an aid in using an ambulatory assist device.

Registrar Corp assists Cane, Tips & Pads companies with:

  • FDA Cane, Tips & Pads Establishment Registration
  • FDA Cane, Tips & Pads Listing
  • FDA Cane, Tips & Pads Label Requirements and Exceptions
  • FDA Cane, Tips & Pads Import Information
  • FDA Cane, Tips & Pads Detentions (Cane, Tips & Pads Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Cane, Tips & Pads Manufacturers (Cane, Tips & Pads Suppliers)
       - Cane, Tips & Pads Distributors
       - Cane, Tips & Pads Processors
       - Cane, Tips & Pads Repackers
       - Cane, Tips & Pads Relabelers
       - Cane, Tips & Pads Exporters
       - Cane, Tips & Pads Importers
For more information about Cane, Tips & Pads 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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2017 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco