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U.S. FDA Medical Device Ossicular Finger Vise Requirements

FDA Medical Device Definition: A prosthesis modification instrument for ossicular replacement surgery is a device intended for use by a surgeon to construct ossicular replacements. This generic type of device includes the ear, nose, and throat cutting block; wire crimper, wire bending die; wire closure forceps; piston cutting jib; gelfoamTMpunch; wire cutting scissors; and ossicular finger vise.

Registrar Corp assists Ossicular Finger Vise companies with:

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