Data / Medical devices / Pin, Fixation, Threaded / Italy
FDA-registered makers of Pin, Fixation, Threaded in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Pin, Fixation, Threaded (product code JDW). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Pin, Fixation, Threaded
- Product code
- JDW
- Country
- Italy
Makers of Pin, Fixation, Threaded in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medicalplastic | MILANO Lombardy, Italy | Specification developer | 2 | June 7, 2012 | 0 | 0 | 0 | api.fda.gov |
| Orthofix SRL | BUSSOLENGO Verona, Italy | Manufacturer | 2 | March 18, 1998 | 0 | 2 | 0 | api.fda.gov |
| Citieffe SRL | Calderara di Reno Bologna, Italy | Manufacturer | 1 | July 7, 2015 | 0 | 0 | 0 | api.fda.gov |
| Hofmann S.R.L. | MONZA (MI) Monza e Brianza, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lincotek Trento S.P.A | Cire di Pergine Trento, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.