Establishment Registration




The following type of establishments:

  1. Contract Manufacturer
  2. Contract Sterilizer
  3. Foreign Exporter
  4. Initial Distributor
  5. Manufacturer
  6. Repackage
  7. Relabelers
  8. Remanufacturer
  9. Preprocessors of Single Use Devices
  10. Specification Developer
  11. U. S. manufacturer of export only devices



involved in the production and distribution of medical devices intended for commercial distribution in the U.S.A are required to register annually with the FDA. Most establishments that are required to register are also required to list the devices.

If a device requires premarket approval or notification before being marketed in the U.S., then the owner/operator should also submit the FDA premarket submission number/510k.

The requirements for registration and listing based on the type of activity performed at that establishment. More details about which types of activities require payment of the establishment registration fee.

Contact us

A1-101, Ankur,
Near Cipla Foundation,
Warje, Pune- 411058

E mail :- info@avscertification.com
Telephone :- +91 - 9881946595



Design & Developed By : Logic Palace Systems and Softwares
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