Data / Medical devices / Prosthesis, Hip, Hemi-, Femoral, Metal / China
FDA-registered makers of Prosthesis, Hip, Hemi-, Femoral, Metal in China: 8 establishments
8 establishments in China are registered with the FDA to make Prosthesis, Hip, Hemi-, Femoral, Metal (product code KWL). 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, Hemi-, Femoral, Metal
- Product code
- KWL
- Country
- China
Makers of Prosthesis, Hip, Hemi-, Femoral, Metal in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou City Jiangsu, China | Contract manufacturer, Manufacturer | 1 | January 19, 1999 | 0 | 0 | 0 | api.fda.gov |
| Canwell Medical Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Synthes (suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MicroPort Orthopedics Global Supply Center Limited | Shanghai, 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 | |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer, 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.