Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / China
FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in China: 5 establishments
5 establishments in China are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Shoulder Prosthesis, Reverse Configuration
- Product code
- PHX
- Country
- China
Makers of Shoulder Prosthesis, Reverse Configuration in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Depuy Synthes (suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, China | Manufacturer | 6 | September 15, 2021 | 0 | 0 | 0 | api.fda.gov |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou City Jiangsu, China | Contract manufacturer, Manufacturer | 5 | February 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer, Manufacturer | 2 | April 15, 2020 | 0 | 0 | 0 | api.fda.gov |
| Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. | Changzhou, Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Trauson (Changzhou) Medical Technology Co., Ltd. | Changzhou City Jiangsu, China | 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.