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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

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 191
  • EUDAMED 188

A device listed in two registries counts in both.

Device classes
  • FDA Class II 179
  • FDA Class I 12
Identifiers
  • DUNS 387588051

At a glance

Counted by deviCERTS from registry records

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.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue191

Newest first, rows 1-50 of 191

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  • Elos Instruments SE256A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Elos Instruments SE259

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Elos Instruments SE258A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Intrauma Surgical Instrument S205

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Wristar Multiax KM1.9031

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9032

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9034

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9035

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9037

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9036

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax KM1.9038

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2308

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2312

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2316

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2320

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2322

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2326

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2324

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2328

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Multiax Screw 120.2330

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax 120.9034

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Wristar Multiax 120.9035

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Intrauma Surgical Instrument S21

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Wristar Multiax 120.9036

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Intrauma Surgical Instrument S215

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S210

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S213

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S222

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S23

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S232

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S235

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S24HL

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S245HL

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Intrauma Surgical Instrument S291

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Wristar Multiax T120.903X

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite 120.7109

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite 120.7111

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite 120.7112

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite 120.7113

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite 120.7114

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Locking Screw 120.2518

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Cortical Screw 120.2732

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos Instruments SE206B

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos Instruments SE213

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite KM2.7109

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos Instruments SE208E

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Kite KM2.7110

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos Instruments SE214

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos 200.1801

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Elos 200.1120

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II

Rows 1-50 of 191

Showing 1-50 of 191

Company details

DUNS number
387588051

FDA establishments1

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

  • 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.

Generated automatically from registry data and not verified by a human reviewer.