Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / United Kingdom
FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 1 has 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
- Shoulder Prosthesis, Reverse Configuration
- Product code
- PHX
- Country
- United Kingdom
Makers of Shoulder Prosthesis, Reverse Configuration in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Depuy Intl., Ltd. | Leeds, United Kingdom | Manufacturer | 1 | December 15, 2010 | 0 | 0 | 0 | api.fda.gov |
| Accentus Medical Ltd | DIDCOT Oxfordshire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Automatics Tooling Company Ltd | Salfords Surrey, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthoplastics Ltd | Bacup Lancashire, United Kingdom | Contract manufacturer | 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 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.