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Browse the catalogue

Medical devices and their regulatory records, by registry, by clinical category (GMDN) or by EMDN group.

The registries

About 9.1M unique devices as of 2026-11-12; a device can be in more than one registry, so the registry counts overlap

  • EUDAMED

    Is this device CE-marked under the MDR or IVDR, and who makes it? The European Commission database lists devices, manufacturers and authorised representatives.

  • FDA 510(k)

    Has the FDA cleared this device as substantially equivalent to one already on the US market?

  • FDA PMA

    Has the FDA approved this high-risk (Class III) device after reviewing its safety and effectiveness?

  • FDA De Novo

    Did the FDA grant this new low- or moderate-risk device, which has no equivalent, a first authorization?

  • FDA GUDID

    Which device identifier (UDI-DI), labeller and model does the FDA list for this product?

In the catalogue

Each registry counted on its own: a device can be in more than one

In the catalogue

Devices by registry

FDA records

  • FDA recalls

    60K

    recall records

  • FDA registrations

    25K

    establishments

Browse by category

Clinical categories from the GMDN nomenclature

All categories

Recently updated manufacturers

All manufacturers

EMDN groups

The top-level groups of the European Medical Device Nomenclature

Recently described devices

All devices

Latest FDA recalls by manufacturer

Manufacturer with the newest recall record

Recently added 510(k) records

Newest records in the catalogue

All 510(k) devices