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Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented / China

FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented in China: 11 establishments

11 establishments in China are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented (product code JDI). 2 have 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, Semi-Constrained, Metal/Polymer, Cemented
Product code
JDI
Country
China

Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Depuy Synthes (suzhou) Medical Devices Co., Ltd.SUZHOU Jiangsu, ChinaManufacturer15July 22, 2022000api.fda.gov
Changzhou Biomet Medical Devices Co., Ltd.Changzhou City Jiangsu, ChinaManufacturer8September 29, 2005000api.fda.gov
APS Materials SuzhouSuzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
B-One Medical (suzhou) Co., Ltd.Suzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Canwell Medical Co., Ltd.Jinhua Zhejiang, ChinaContract manufacturer0000api.fda.gov
MicroPort Orthopedics Global Supply Center LimitedShanghai, ChinaContract manufacturer0000api.fda.gov
Stryker (Suzhou) Medical Technology Co.,Ltd.Suzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Suzhou Elite Precision Machinery Co., Ltd.Kunshan Jiangsu, ChinaContract manufacturer0000api.fda.gov
Xian Airfoil Technology Co., Ltd.Xian Shaanxi, ChinaContract manufacturer0000api.fda.gov
Zhejiang Biomet Medical Products Co., Ltd.Jinhua Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
b-ONE Medical (Beijing) Co., Ltd.Beijing, ChinaContract manufacturer0000api.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.