Data / Medical devices / Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer / Ireland
FDA-registered makers of Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer in Ireland: 12 establishments
12 establishments in Ireland are registered with the FDA to make Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer (product code MBH). 7 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, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- Product code
- MBH
- Country
- Ireland
Makers of Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Howmedica International S. De R.L. | LIMERICK Munster, Ireland | Manufacturer | 12 | October 24, 2025 | 0 | 0 | 0 | api.fda.gov |
| Stryker Ireland Osteonics | County Cork, Ireland | Manufacturer, Specification developer | 8 | August 15, 2019 | 0 | 0 | 0 | api.fda.gov |
| Depuy Ireland UC | Co. Cork Munster, Ireland | Manufacturer, Specification developer | 6 | June 18, 2024 | 0 | 0 | 0 | api.fda.gov |
| Zimmer Orthopedics Manufacturing Limited-Galway | Oranmore Galway(County), Ireland | Manufacturer | 6 | October 29, 2024 | 0 | 0 | 0 | api.fda.gov |
| Zimmer Orthopedic Mfg Ltd | Shannon Clare, Ireland | Manufacturer | 4 | May 17, 2018 | 0 | 0 | 0 | api.fda.gov |
| Depuy (ireland) | CO. CORK Munster, Ireland | Manufacturer, Specification developer | 2 | February 13, 2015 | 0 | 0 | 0 | api.fda.gov |
| Signature Orthopaedics Europe Ltd | Athlone Westmeath, Ireland | Manufacturer | 1 | December 23, 2025 | 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 | |
| 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 |
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.