Data / Medical devices / Screw, Fixation, Bone / United Kingdom
FDA-registered makers of Screw, Fixation, Bone in the United Kingdom: 9 establishments
9 establishments in the United Kingdom are registered with the FDA to make Screw, Fixation, Bone (product code HWC). 3 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
- Screw, Fixation, Bone
- Product code
- HWC
- Country
- United Kingdom
Makers of Screw, Fixation, Bone in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Biocomposites Ltd. | Keele Staffordshire, United Kingdom | Manufacturer | 3 | August 31, 2007 | 0 | 0 | 0 | api.fda.gov |
| Ortho Solutions UK Limited | Maldon Essex, United Kingdom | Complaint file establishment, Manufacturer, Specification developer | 2 | March 8, 2017 | 0 | 1 | 0 | api.fda.gov |
| Innovate Orthopaedics Ltd. | Huddersfield Kirklees, United Kingdom | Manufacturer | 1 | December 30, 2021 | 0 | 0 | 0 | api.fda.gov |
| Automatics Tooling Company Ltd | Salfords Surrey, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy CMW | Blackpool, Lancashire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Intl., Ltd. | Leeds, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sheffield Precision Medical Ltd | Sheffield, 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 | |
| XL Precision Technologies Ltd | Stockton on Tees Stockton-on-Tees, 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.