Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented / Italy
FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in Italy: 11 establishments
11 establishments in Italy are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented (product code LPH). 2 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
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Product code
- LPH
- Country
- Italy
Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Limacorporate S.p.A. | Villanova di San Daniele Udine, Italy | Manufacturer | 8 | August 29, 2025 | 0 | 1 | 0 | api.fda.gov |
| Adler Ortho S.P.A. | Cormano Milano, Italy | Manufacturer | 1 | January 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Adler Ortho SpA | Mezzolombardo Trento, Italy | Contract 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 | |
| HPF S.R.L. | Forgaria nel Friuli Friuli Venezia Giulia, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lincotek Bologna S.R.L. | Cadriano di Granarolo, Bologna, 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 | |
| Limacorporate S.p.A. | Calatafimi Segesta (TP) Sicilia, Italy | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oeb S.R.L. | Camposanto Modena, Italy | Contract 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 | |
| Valtecne SPA | Berbenno di Valtellina Sondrio, 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.