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Data / Medical devices / Instrument, Ent Manual Surgical / United Kingdom

FDA-registered makers of Instrument, Ent Manual Surgical in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Instrument, Ent Manual Surgical (product code LRC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Instrument, Ent Manual Surgical
Product code
LRC
Country
United Kingdom

Makers of Instrument, Ent Manual Surgical in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bailey Instruments LtdManchester, United KingdomManufacturer0000api.fda.gov
DTR Medical LtdSwansea, United KingdomManufacturer0000api.fda.gov
Exmoor Plastics LimitedChorley Lancashire, United KingdomManufacturer0000api.fda.gov
Haag-Streit Uk Ltd.Bishop's Stortford Hertfordshire, United KingdomManufacturer0000api.fda.gov
Robinson Healthcare LimitedWorksop Nottinghamshire, United KingdomManufacturer0000api.fda.gov
Sheffmed LimitedRotherham, United KingdomManufacturer0000api.fda.gov
Surtex Instruments LtdLondon Surrey, United KingdomManufacturer0000api.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.