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Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate / Ireland

FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate in Ireland: 10 establishments

10 establishments in Ireland are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate (product code MEH). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Product code
MEH
Country
Ireland

Makers of Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Stryker Ireland OsteonicsCounty Cork, IrelandManufacturer, Specification developer16August 11, 2022000api.fda.gov
Signature Orthopaedics Europe LtdAthlone Westmeath, IrelandContract manufacturer, Manufacturer7November 25, 2024010api.fda.gov
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Repackager or relabeler, Specification developer5January 19, 2024000api.fda.gov
Depuy Ireland UCCo. Cork Munster, IrelandManufacturer, Specification developer4January 19, 2024000api.fda.gov
Howmedica International S. De R.L.LIMERICK Munster, IrelandManufacturer2September 28, 2011000api.fda.gov
Aps Materials Inc. IrelandWaterford Waterford(County), IrelandContract manufacturer0000api.fda.gov
Caragh PrecisionGalway Galway(County), IrelandContract manufacturer0000api.fda.gov
Smithstown Light EngineeringShannon Clare, IrelandContract manufacturer0000api.fda.gov
Symmetry Medical Ireland LimitedMidleton, Cork Munster, IrelandContract manufacturer0000api.fda.gov
Stryker AnngroveCork Munster, IrelandContract manufacturer0000api.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.