Data / Medical devices / Rod, Fixation, Intramedullary And Accessories / Italy
FDA-registered makers of Rod, Fixation, Intramedullary And Accessories in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Rod, Fixation, Intramedullary And Accessories (product code HSB). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Rod, Fixation, Intramedullary And Accessories
- Product code
- HSB
- Country
- Italy
Makers of Rod, Fixation, Intramedullary And Accessories in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Orthofix SRL | BUSSOLENGO Verona, Italy | Exporter to the US, Manufacturer | 15 | May 19, 2026 | 0 | 1 | 0 | api.fda.gov |
| Citieffe SRL | Calderara di Reno Bologna, Italy | Manufacturer | 5 | October 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Intrauma | Bruino Torino, Italy | Manufacturer | 1 | July 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Foreasytech S.R.L. | Settimo di Pescantina Verona, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leghe Leggere Lavorate SRL | buccinasco Milano, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.