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Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Ireland

FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Ireland: 9 establishments

9 establishments in Ireland are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 5 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
Electrosurgical, Cutting & Coagulation & Accessories
Product code
GEI
Country
Ireland

Makers of Electrosurgical, Cutting & Coagulation & Accessories in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Stryker Ireland Ltd. Instruments Division, Innovation CentreCarrigtwohill Cork(County), IrelandSpecification developer10September 17, 2026000api.fda.gov
Boston Scientific LimitedGALWAY Galway(County), IrelandManufacturer3April 17, 2014000api.fda.gov
Neurent Medical LtdGalway Galway(County), IrelandComplaint file establishment, Manufacturer, Specification developer3June 16, 2026000api.fda.gov
Clearstream Technologies Ltd.Wexford, IrelandManufacturer2October 17, 2022000api.fda.gov
Merit Medical Ireland, LtdGalway Galway(County), IrelandContract manufacturer, Repackager or relabeler1August 11, 2010000api.fda.gov
Boston Scientific LimitedCORK Munster, IrelandManufacturer0000api.fda.gov
SchivoWaterford Waterford(City And County), IrelandContract manufacturer0000api.fda.gov
Stryker Ireland Ltd., Instruments DivisionCARRIGTWOHILL, CO.CORK Munster, IrelandContract manufacturer0000api.fda.gov
Utah Medical Products, Ltd.ATHLONE CO. Leinster, 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.