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Data / Medical devices / Component, Traction, Non-Invasive / China

FDA-registered makers of Component, Traction, Non-Invasive in China: 14 establishments

14 establishments in China are registered with the FDA to make Component, Traction, Non-Invasive (product code KQZ). 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
Component, Traction, Non-Invasive
Product code
KQZ
Country
China

Makers of Component, Traction, Non-Invasive in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Changsha Nice Medical Instrument Limited CompanyChangsha Hunan, ChinaManufacturer0000api.fda.gov
Changsha Yuhong Trading Co., Ltd.Changsha Hunan, ChinaManufacturer0000api.fda.gov
Dongguan Ness Sports Technology Co., Ltd.Dongguan Guangdong, ChinaManufacturer0000api.fda.gov
Guangzhou Xinbo Electronic Co., Ltdguangzhou Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Hebei Junlaole Medical Technology Co.,ltdHengshui City Hebei, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiaxing Huaqin Medical Industrial Co., Ltd.Ping Hu Zhejiang, ChinaManufacturer0000api.fda.gov
Ningbo Ningyuan Import & Export Co., Ltd.Ningbo, Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Shanghai Huihu Medical Appliance Co. Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Shanghai Nuofeng Medical Technology Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Shenzhen Obestec Industrial Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shanghai Xodus Medical Company LimitedShanghai, ChinaManufacturer0000api.fda.gov
Suzhou Elite Precision Machinery Co., Ltd.Kunshan Jiangsu, ChinaContract manufacturer0000api.fda.gov
Zhejiang Mediunion Healthcare Group Co.,ltdNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
Zhongshan A&e Machinery Industry Co., LtdZhongshan City Guangdong, 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.