Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate / United Kingdom
FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate in the United Kingdom: 6 establishments
6 establishments in the United Kingdom are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate (product code MEH). 3 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, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- Product code
- MEH
- Country
- United Kingdom
Makers of Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Corin Limited | CIRENCESTER Gloucestershire, United Kingdom | Complaint file establishment, Manufacturer | 5 | August 10, 2026 | 0 | 3 | 0 | api.fda.gov |
| Implants Intl. Ltd. | THORNABY-ON-TEES Stockton-on-Tees, United Kingdom | Manufacturer | 2 | July 25, 2007 | 0 | 0 | 0 | api.fda.gov |
| Depuy Intl., Ltd. | Leeds, United Kingdom | Manufacturer, Specification developer | 1 | January 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Accentus Medical Ltd | DIDCOT Oxfordshire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomet Uk Ltd. | Bridgend, United Kingdom | 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 |
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.