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Data / Medical devices / Board, Arm (With Cover), Non-Sterile / China

FDA-registered makers of Board, Arm (With Cover), Non-Sterile in China: 11 establishments

11 establishments in China are registered with the FDA to make Board, Arm (With Cover), Non-Sterile (product code NOD). 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
Board, Arm (With Cover), Non-Sterile
Product code
NOD
Country
China

Makers of Board, Arm (With Cover), Non-Sterile in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aimmax Medical Products Co.,ltd.Shiyan Hubei, ChinaContract manufacturer0000api.fda.gov
Anqing Clean Dental Instrument Technology Co.,ltdAnqing City Anhui, ChinaExporter to the US, Manufacturer0000api.fda.gov
Beijing Demax Medical Technology Co., Ltd.Beijing, ChinaManufacturer0000api.fda.gov
Brady (Xiamen) Co. Ltd.Xiamen Fujian, ChinaContract manufacturer0000api.fda.gov
Dongguan City Fenglinwan Leisure Products Co., Ltd.Dongguan City Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Jiangyin PuremedJiangyin Jiangsu, ChinaContract manufacturer0000api.fda.gov
Jiangyin Huaying Light Industrial Products Co., LTDJiangyin Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Lingxian Dongsheng Textile Co., Ltd.Dezhou Shandong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Ningbo Ningyuan Import & Export Co., Ltd.Ningbo, Zhejiang, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Tianjin Demax Medical Technology Co., Ltd.Tianjin, ChinaContract manufacturer0000api.fda.gov
Xiantao Daoqi Plastic Co., Ltd.Xiantao Hubei, 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.