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Data / Medical devices / Passer, Wire, Orthopedic / China

FDA-registered makers of Passer, Wire, Orthopedic in China: 7 establishments

7 establishments in China are registered with the FDA to make Passer, Wire, Orthopedic (product code HXI). 0 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
Passer, Wire, Orthopedic
Product code
HXI
Country
China

Makers of Passer, Wire, Orthopedic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aplus (guangzhou) Medical Technology CompanyGuangzhou Guangdong, ChinaContract manufacturer0000api.fda.gov
Changzhou Centrau Medical Instrument Co.,ltd.CHANGZHOU Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Changzhou Wastonortho Medical Appliance Co., Ltd.Changzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Double Medical Technology Inc.Xiamen Fujian, ChinaContract manufacturer0000api.fda.gov
SHANGHAI KiNETIC MEDICAL CO LTDShanghai, ChinaContract manufacturer0000api.fda.gov
Shanghai Medical Instruments (group) Ltd. Corp.Shanghai, ChinaManufacturer0000api.fda.gov
Suzhou Endophix Co., Ltd.Suzhou Jiangsu, ChinaManufacturer0000api.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.