Intrauma SpA
Country not established FDA
Intrauma SpA is a medical device manufacturer, with 191 devices listed in FDA GUDID and EUDAMED (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 191
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 191
- EUDAMED 188
- Device classes
- FDA Class II 179
- FDA Class I 12
- Identifiers
- DUNS 387588051
At a glance
Market reach
- United States
- FDA establishment
What Intrauma SpA makes
Intrauuma SPA manufactures orthopaedic fixation devices, including non-sliding bone screws, femur intramedullary nails, and non-bioabsorbable screws and plates for surgical stabilization. Their portfolio also includes reusable surgical tools such as drill guides, fluted drill bits, and medical rulers, as well as orthopaedic implant aiming arms for precision alignment during procedures.
All listed devices fall under FDA Class II regulation and are recorded in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable medical device compliance standards for orthopaedic hardware.
Catalogue
Search and filter all 191 devicesShowing 1-50 of 191
Company details
- DUNS number
- 387588051
FDA establishments
- Intrauma Bruino Torino · IT FEI 3010502940
Frequently asked questions
How many devices does INTRAUMA SPA have in the registry?
The registry currently lists 191 devices for INTRAUMA SPA. Devices recorded under merged duplicate company entries are counted once.
Which registries list INTRAUMA SPA's devices?
Among its 50 most recently registered devices, INTRAUMA SPA has devices listed in EUDAMED (47 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do INTRAUMA SPA's devices fall under?
Among its 50 most recently registered devices, the classes recorded for INTRAUMA SPA's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from INTRAUMA SPA in the registry?
The most recently registered devices listed for INTRAUMA SPA include ELOS INSTRUMENTS SE256A, ELOS INSTRUMENTS SE259, ELOS INSTRUMENTS SE258A and INTRAUMA SURGICAL INSTRUMENT S205.
Which FDA establishments are linked to INTRAUMA SPA?
1 FDA establishment is linked to INTRAUMA SPA in the registry; they are listed on the company page.