Data / Medical devices / Wire, Surgical / Ireland
FDA-registered makers of Wire, Surgical in Ireland: 5 establishments
5 establishments in Ireland are registered with the FDA to make Wire, Surgical (product code LRN). 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
- Wire, Surgical
- Product code
- LRN
- Country
- Ireland
Makers of Wire, Surgical in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Ireland Osteonics | County Cork, Ireland | Manufacturer | 1 | April 23, 1990 | 0 | 0 | 0 | api.fda.gov |
| Depuy (ireland) | CO. CORK Munster, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Ireland UC | Co. Cork Munster, Ireland | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Howmedica International S. De R.L. | LIMERICK Munster, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Anngrove | Cork Munster, 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.