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Data / Medical devices / Extractor / China

FDA-registered makers of Extractor in China: 14 establishments

14 establishments in China are registered with the FDA to make Extractor (product code HWB). 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
Extractor
Product code
HWB
Country
China

Makers of Extractor in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Apex (Guangzhou) Tools & Orthopedics CompanyGuangzhou Guangdong, ChinaContract manufacturer0000api.fda.gov
Autocam Medical Devices (Suzhou) Co. Ltd.Suzhou 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
Changzhou Geasure Medical Apparatus And Instruments Co., LtdChangzhou Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Guangzhou Aquila Precise Tools LimitedGuangzhou City Guangdong, ChinaContract manufacturer0000api.fda.gov
Medtronic (Changzhou) Medical Devices Technology Co., LtdChangzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Saferlife Products Co.,ltd.Guangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Shanghai Medical Instruments (group) Ltd. Corp.Shanghai, ChinaManufacturer0000api.fda.gov
Suzhou Microport Orthorecon Co., Ltd.Suzhou Jiangsu, ChinaComplaint file establishment, Contract manufacturer, Repackager or relabeler0000api.fda.gov
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd.Changzhou, Jiangsu, ChinaContract manufacturer0000api.fda.gov
Turnxon Precision Co., LtdDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Xinhua Healthcare Industry Co.,limitedZibo Shandong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhejiang Biomet Medical Products Co., Ltd.Jinhua Zhejiang, ChinaContract manufacturer, 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.