Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented / China
FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented in China: 13 establishments
13 establishments in China are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented (product code LPH). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Product code
- LPH
- Country
- China
Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented 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 | 10 | May 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Depuy Synthes (suzhou) Medical Devices Co., Ltd. | SUZHOU Jiangsu, China | Manufacturer | 9 | October 21, 2020 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua Zhejiang, China | Contract manufacturer, Manufacturer | 7 | October 6, 2015 | 0 | 0 | 0 | api.fda.gov |
| Beijing Ikey Medical Device Technology Co., Ltd. | Beijing, China | Manufacturer | 1 | May 14, 2020 | 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 | |
| Guangzhou Aquila Precise Tools Limited | Guangzhou City Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lincotek (wuxi) Co., Ltd. | Wuxi Jiangsu, China | Contract 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 | |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou 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 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.