Data / Medical devices / Orthopedic Manual Surgical Instrument / United Kingdom
FDA-registered makers of Orthopedic Manual Surgical Instrument in the United Kingdom: 17 establishments
17 establishments in the United Kingdom are registered with the FDA to make Orthopedic Manual Surgical Instrument (product code LXH). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Orthopedic Manual Surgical Instrument
- Product code
- LXH
- Country
- United Kingdom
Makers of Orthopedic Manual Surgical Instrument in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arthro Dynamik Ltd | Wetherby York, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biocomposites Ltd. | Keele Staffordshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomet Uk Ltd. | Bridgend, United Kingdom | Specification developer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Bradford Tool Group | Bradford York, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bailey Instruments Ltd | Manchester, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Claro Precision Eng Ltd | Knaresborough North Yorkshire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clinical Polymer Technologies Ltd | Coalville Leicestershire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Corin Limited | CIRENCESTER Gloucestershire, United Kingdom | Complaint file establishment, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Intl., Ltd. | Leeds, United Kingdom | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eventum Orthopaedics Ltd | Leeds, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kirkstall Precision Ltd | Leeds, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Osteotec Limited | Newbury West Berkshire, United Kingdom | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ortho Solutions UK Limited | Maldon Essex, United Kingdom | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sheffield Precision Medical Ltd | Sheffield, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Summit Medical Ltd. | Gloucestershire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetry Medical Thornton Precision Components Ltd | SHEFFIELD, SOUTH YORKSHIRE Barnsley, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgical Specialties Corporation Limited (UK) | Taunton Somerset, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.