Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Ophthalmic Trial Frame Regulations

U.S. FDA Medical Device Ophthalmic Trial Frame Requirements


FDA Medical Device Definition: An opthalmic trial lens frame is a mechanical device intended to hold trial lenses for vision testing.

Registrar Corp assists Ophthalmic Trial Frame companies with:

  • FDA Ophthalmic Trial Frame Establishment Registration
  • FDA Ophthalmic Trial Frame Listing
  • FDA Ophthalmic Trial Frame Label Requirements and Exceptions
  • FDA Ophthalmic Trial Frame Import Information
  • FDA Ophthalmic Trial Frame Detentions (Ophthalmic Trial Frame Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Ophthalmic Trial Frame Manufacturers (Ophthalmic Trial Frame Suppliers)
       - Ophthalmic Trial Frame Distributors
       - Ophthalmic Trial Frame Processors
       - Ophthalmic Trial Frame Repackers
       - Ophthalmic Trial Frame Relabelers
       - Ophthalmic Trial Frame Exporters
       - Ophthalmic Trial Frame Importers
For more information about Ophthalmic Trial Frame 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 © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco