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Data / Medical devices / Chair, Geriatric / China

FDA-registered makers of Chair, Geriatric in China: 11 establishments

11 establishments in China are registered with the FDA to make Chair, Geriatric (product code FRJ). 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
Chair, Geriatric
Product code
FRJ
Country
China

Makers of Chair, Geriatric in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A & I Industries LtdFOSHAN CITY Guangdong, ChinaManufacturer0000api.fda.gov
Danyang Huayi Medical Supply & Equipment Co, LtdDANYANG Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Jiangsu Pinkang Medical Technology Co LtdDanyang Jiangsu, ChinaContract manufacturer0000api.fda.gov
Jiangyin Unixcare Medical Devices Co.,ltdJiangyin Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiaxing Kalanchoe Medical Technology Co., LtdJiaxing Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Jan Mao Industries Co., Ltd.Guangxi Zhuang Autonomous Region, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiangsu Intco Medical Products Co., Ltd.Zhenjiang New District Jiangsu, ChinaManufacturer0000api.fda.gov
Jiangyin Huashi Medical Equipment Co.,LtdJiangyin City Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Yongkang Beiqin Industry & Trade Co.,ltdYongkang Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Zhejiang Kelongwei Medical Equipment Co., Ltd.Shaoxing Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhongshan A&j Medical Equipment Co., Ltd. (JBS)Zhongshan 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.