Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented / Ireland
FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in Ireland: 13 establishments
13 establishments in Ireland are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented (product code LPH). 5 have a 510(k) clearance or PMA approval on file and 0 have 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
- Ireland
Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Ireland Osteonics | County Cork, Ireland | Manufacturer, Specification developer | 21 | July 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Depuy (ireland) | CO. CORK Munster, Ireland | Manufacturer, Repackager or relabeler, Specification developer | 12 | October 21, 2020 | 0 | 0 | 0 | api.fda.gov |
| Depuy Ireland UC | Co. Cork Munster, Ireland | Manufacturer, Specification developer | 9 | January 22, 2025 | 0 | 0 | 0 | api.fda.gov |
| Howmedica International S. De R.L. | LIMERICK Munster, Ireland | Manufacturer | 6 | December 21, 2023 | 0 | 0 | 0 | api.fda.gov |
| Signature Orthopaedics Europe Ltd | Athlone Westmeath, Ireland | Manufacturer | 2 | July 22, 2014 | 0 | 0 | 0 | api.fda.gov |
| Aps Materials Inc. Ireland | Waterford Waterford(County), Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caragh Precision | Galway Galway(County), Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nelipak Healthcare Packaging | CLARA, Offaly, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smithstown Light Engineering | Shannon Clare, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetry Medical Ireland Limited | Midleton, Cork Munster, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Anngrove | Cork Munster, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Takumi Precision Engineering Ltd | Limerick Limerick(County), Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer Orthopedics Manufacturing Limited-Galway | Oranmore Galway(County), Ireland | 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.