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HomeMedical Devices › U.S. FDA Medical Device Establishment Registration, Listings and U.S. Agent Requirements › Register Medical Device Establishment With The U.S. FDA

U.S. FDA Medical Device Establishment Registration, Listings and U.S. Agent Requirements

Step 1

The form below will assist you with fulfilling U.S. FDA's Medical Device requirements, including payment of U.S. FDA government fees (if required).

Filing Options: Process Online
Send me forms to file by Fax or Mail
Company Name: *
Contact Person Name: *
Physical Address: *
City: *
State/Province/Region:
Country: *
Postal Code:
Phone: *
Mobile:
Fax:
E-mail: *
Website:
FDA Medical Device Establishment#:
FDA Medical Device Owner/Operator#:
We are registered but I cannot recall our Registration or Owner/Operator Number






 
U.S. FDA Regulations:

U.S. FDA Medical Device Regulation: 21 C.F.R. Part 801 et seq.



















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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