Data / Medical devices / Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented / Ireland
FDA-registered makers of Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented in Ireland: 8 establishments
8 establishments in Ireland are registered with the FDA to make Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented (product code HSD). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
- Product code
- HSD
- Country
- Ireland
Makers of Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented 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 | 4 | March 26, 2004 | 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 | |
| Depuy (ireland) | CO. CORK Munster, Ireland | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Ireland UC | Co. Cork Munster, Ireland | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Ireland Osteonics | County Cork, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Macroom | Co Cork Munster, Ireland | Contract manufacturer, 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 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.