Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Intraoral Dental Drill Regulations

U.S. FDA Medical Device Intraoral Dental Drill Requirements


FDA Medical Device Definition: An intraoral dental drill is a rotary device intended to be attached to a dental handpiece to drill holes in teeth to secure cast or preformed pins to retain operative dental appliances.

Registrar Corp assists Intraoral Dental Drill companies with:

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