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Data / Medical devices / Fastener, Fixation, Nondegradable, Soft Tissue / United Kingdom

FDA-registered makers of Fastener, Fixation, Nondegradable, Soft Tissue in the United Kingdom: 6 establishments

6 establishments in the United Kingdom are registered with the FDA to make Fastener, Fixation, Nondegradable, Soft Tissue (product code MBI). 3 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
Fastener, Fixation, Nondegradable, Soft Tissue
Product code
MBI
Country
United Kingdom

Makers of Fastener, Fixation, Nondegradable, Soft Tissue in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Lockdown Medical LimitedRedditch Worcestershire, United KingdomManufacturer1June 13, 2008000api.fda.gov
Summit Medical Ltd.Gloucestershire, United KingdomManufacturer1July 25, 2017000api.fda.gov
Xiros LtdYEADON Leeds, United KingdomManufacturer1September 9, 2015000api.fda.gov
Entaco Ltd.Redditch Worcestershire, United KingdomContract manufacturer0000api.fda.gov
Surgical Specialties Corporation Limited (UK)Taunton Somerset, United KingdomContract manufacturer0000api.fda.gov
XL Precision Technologies LtdStockton on Tees Stockton-on-Tees, United KingdomContract manufacturer, Exporter to the US0000api.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.