Establishment Registration & Device Listing
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This database includes:
- medical device manufacturers registered with FDA and
- medical devices listed with FDA
Need to update your information? To modify, add, or delete information, log onto your FURLS account.
The changes will appear in the public registration and listing database when it is updated. Please note: There is a delay between the time that the data is uploaded and the time that the data appears in the public registration and listing database. Existing device listings may also be effected by the update and may not be fully viewable until after the update has been completed. Updates are generally completed weekly by Monday evening.
* Category includes Countries, States and Regions
Other Databases
- 510(k)s
- De Novo
- Medical Device Reports (MAUDE)
- CDRH Export Certificate Validation (CECV)
- CDRH FOIA Electronic Reading Room
- CFR Title 21
- CLIA
- Device Classification
- FDA Guidance Documents
- Humanitarian Device Exemption
- Medsun Reports
- Premarket Approvals (PMAs)
- Post-Approval Studies
- Postmarket Surveillance Studies
- Radiation-Emitting Products
- Radiation-Emitting Electronic Products Corrective Actions
- Recalls
- Standards
- Total Product Life Cycle
- X-Ray Assembler
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