Data / Medical devices / Orthopedic Manual Surgical Instrument / Italy
FDA-registered makers of Orthopedic Manual Surgical Instrument in Italy: 18 establishments
18 establishments in Italy are registered with the FDA to make Orthopedic Manual Surgical Instrument (product code LXH). 0 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
- Orthopedic Manual Surgical Instrument
- Product code
- LXH
- Country
- Italy
Makers of Orthopedic Manual Surgical Instrument in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Adler Ortho S.P.A. | Cormano Milano, Italy | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biopsybell S.R.L. | MIRANDOLA Modena, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BRM Extremities SRL | Civate (LC) Lombardy, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Citieffe SRL | Calderara di Reno Bologna, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Den Tag S.R.L. | MANIAGO, PN. Pordenone, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eddi Bressan S.R.L. | CORMONS Gorizia, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| G21 S.R.I. | San Possidonio Modena, Italy | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HPF S.R.L. | Forgaria nel Friuli Friuli Venezia Giulia, Italy | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intrauma | Bruino Torino, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leghe Leggere Lavorate SRL | buccinasco Milano, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Limacorporate S.p.A. | Villanova di San Daniele Udine, Italy | Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| MDP SRL | Artegna Udine, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medicalplastic | MILANO Lombardy, Italy | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NCS Lab SRL | Carpi Modena, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oeb S.R.L. | Camposanto Modena, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthofix SRL | BUSSOLENGO Verona, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sti Lualdi S.R.L. | Casiacco Pordenone, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tecres SPA | VERONA Veneto, Italy | Exporter to the US, 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.