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Data / Medical devices / Orthosis, Limb Brace / United Kingdom

FDA-registered makers of Orthosis, Limb Brace in the United Kingdom: 8 establishments

8 establishments in the United Kingdom are registered with the FDA to make Orthosis, Limb Brace (product code IQI). 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
Orthosis, Limb Brace
Product code
IQI
Country
United Kingdom

Makers of Orthosis, Limb Brace in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Culzean Textile Solutions LtdIrvine North Ayrshire, United KingdomContract manufacturer0000api.fda.gov
Cuxson Gerrard & Co., Ltd.OLDBURY Sandwell, United KingdomManufacturer0000api.fda.gov
DM Orthotics LtdRedruth Cornwall, United KingdomManufacturer0000api.fda.gov
FuzerxLondon Southwark, United KingdomManufacturer0000api.fda.gov
Narcissus RisingFerndown Dorset, United KingdomManufacturer0000api.fda.gov
Neo G LimitedKnaresborough North Yorkshire, United KingdomManufacturer0000api.fda.gov
Promedics Orthopaedic LtdPort Glasgow Scotland, United KingdomComplaint file establishment, Manufacturer0000api.fda.gov
Trulife, Ltd.S. Yorkshire Sheffield, 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.