Data / Medical devices / Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer / China
FDA-registered makers of Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer in China: 8 establishments
8 establishments in China are registered with the FDA to make Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer (product code KWZ). 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
- Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
- Product code
- KWZ
- Country
- China
Makers of Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer, Manufacturer | 1 | January 23, 2003 | 0 | 0 | 0 | api.fda.gov |
| APS Materials Suzhou | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Canwell Medical Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou City Jiangsu, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lincotek (wuxi) Co., Ltd. | Wuxi Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker (Suzhou) Medical Technology Co.,Ltd. | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xian Airfoil Technology Co., Ltd. | Xian Shaanxi, 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.