ORTHOKEY ITALIA SRL

US Last updated 30 May 2026 Part of Orthokey Italia SRL

Devices: 5
Registries: GUDIDFDA
FDA recalls: 0

Catalogue5

Perseus 20904601 Ref 20904601

Class II FDA UDI Active
Perseus 300110278 Ref 300110278

Class II FDA UDI Active
Perseus 300110379 Ref 300110379

Class II FDA UDI Active
Perseus 300110144 Ref 300110144

Class II FDA UDI Active
Perseus 300110198 Ref 300110198

Class II FDA UDI Active

FDA establishments1

Registered with the FDA under this company group, matched by name.

Orthokey Italia SRL Firenze · IT FEI 3020983478

What ORTHOKEY ITALIA SRL makes

OrthoKey Italia Srl manufactures reusable, non-medicated orthopaedic surgical procedure kits designed for specific surgical applications. The kits include the Perseus system, which appears to be a standardized set of tools and instruments for orthopaedic procedures.

These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable medical device regulations for surgical instrumentation.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Website: orthokey.eu
Email: [email protected]
Phone: +39 055354829
DUNS number: 433594191

Catalogue5

Perseus 20904601 Ref 20904601

Perseus 300110278 Ref 300110278

Perseus 300110379 Ref 300110379

Perseus 300110144 Ref 300110144

Perseus 300110198 Ref 300110198

FDA establishments1

What ORTHOKEY ITALIA SRL makes

Information