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Data / Medical devices / Orthopedic Manual Surgical Instrument / Ireland

FDA-registered makers of Orthopedic Manual Surgical Instrument in Ireland: 12 establishments

12 establishments in Ireland are registered with the FDA to make Orthopedic Manual Surgical Instrument (product code LXH). 0 have 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
Orthopedic Manual Surgical Instrument
Product code
LXH
Country
Ireland

Makers of Orthopedic Manual Surgical Instrument in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Caragh PrecisionGalway Galway(County), IrelandContract manufacturer0000api.fda.gov
Croom Precision MedicalCroom Limerick(County), IrelandContract manufacturer0000api.fda.gov
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Depuy Ireland UCCo. Cork Munster, IrelandManufacturer, Specification developer0000api.fda.gov
Howmedica International S. De R.L.LIMERICK Munster, IrelandManufacturer0000api.fda.gov
Nelipak Healthcare PackagingCLARA, Offaly, IrelandContract manufacturer0000api.fda.gov
OrthoxelCork Cork(City), IrelandComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Smithstown Light EngineeringShannon Clare, IrelandContract manufacturer0000api.fda.gov
Stryker Ireland OsteonicsCounty Cork, IrelandManufacturer0000api.fda.gov
Symmetry Medical Ireland LimitedMidleton, Cork Munster, IrelandContract manufacturer0000api.fda.gov
Signature Orthopaedics Europe LtdAthlone Westmeath, IrelandManufacturer, Specification developer0000api.fda.gov
Takumi Precision Engineering LtdLimerick Limerick(County), 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.