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Data / Medical devices / Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer / United Kingdom

FDA-registered makers of Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer in the United Kingdom: 9 establishments

9 establishments in the United Kingdom are registered with the FDA to make Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer (product code JWH). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Product code
JWH
Country
United Kingdom

Makers of Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Corin LimitedCIRENCESTER Gloucestershire, United KingdomComplaint file establishment, Manufacturer6September 23, 2024030api.fda.gov
Depuy Intl., Ltd.Leeds, United KingdomManufacturer, Specification developer2March 29, 1989000api.fda.gov
Implants Intl. Ltd.THORNABY-ON-TEES Stockton-on-Tees, United KingdomManufacturer1November 6, 1998000api.fda.gov
Matortho LimitedLeatherhead Surrey, United KingdomManufacturer1November 17, 2014000api.fda.gov
MatOrtho LimitedPlymouth Devon, United KingdomManufacturer1November 17, 2014000api.fda.gov
Biocomposites Ltd.Keele Staffordshire, United KingdomSpecification developer0000api.fda.gov
Orthoplastics LtdBacup Lancashire, United KingdomContract manufacturer0000api.fda.gov
Sheffield Precision Medical LtdSheffield, United KingdomContract manufacturer0000api.fda.gov
Symmetry Medical Thornton Precision Components LtdSHEFFIELD, SOUTH YORKSHIRE Barnsley, United KingdomContract 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.