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Data / Medical devices / Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment / Ireland

FDA-registered makers of Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment in Ireland: 6 establishments

6 establishments in Ireland are registered with the FDA to make Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment (product code HWE). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Product code
HWE
Country
Ireland

Makers of Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Specification developer0000api.fda.gov
Depuy Ireland UCCo. Cork Munster, IrelandSpecification developer0000api.fda.gov
Smithstown Light EngineeringShannon Clare, IrelandContract manufacturer0000api.fda.gov
Stryker Ireland Ltd., Instruments DivisionCARRIGTWOHILL, CO.CORK Munster, IrelandContract manufacturer0000api.fda.gov
Stryker Ireland Ltd. Instruments Division, Innovation CentreCarrigtwohill Cork(County), IrelandSpecification developer0000api.fda.gov
Takumi Precision Engineering LtdLimerick Limerick(County), IrelandContract manufacturer0000api.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.