Data / Medical devices / Plate, Fixation, Bone / United Kingdom
FDA-registered makers of Plate, Fixation, Bone in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Plate, Fixation, Bone (product code HRS). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Plate, Fixation, Bone
- Product code
- HRS
- Country
- United Kingdom
Makers of Plate, Fixation, Bone in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ortho Solutions UK Limited | Maldon Essex, United Kingdom | Complaint file establishment, Manufacturer, Specification developer | 4 | April 13, 2021 | 0 | 0 | 0 | api.fda.gov |
| Depuy CMW | Blackpool, Lancashire, United Kingdom | Manufacturer | 1 | July 15, 2008 | 0 | 0 | 0 | api.fda.gov |
| Automatics Tooling Company Ltd | Salfords Surrey, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Invibio Device Component Manufacturing, Ltd. (idcm Ltd.) | Thornton Cleveleys Lancashire, 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.