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Data / Medical devices / Armboard, Wheelchair / China

FDA-registered makers of Armboard, Wheelchair in China: 14 establishments

14 establishments in China are registered with the FDA to make Armboard, Wheelchair (product code IMY). 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
Armboard, Wheelchair
Product code
IMY
Country
China

Makers of Armboard, Wheelchair in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anhui Yibao Home Textile Co.,ltdHefei Anhui, ChinaManufacturer0000api.fda.gov
China Wonderland Nurserygoods Co., Ltd.Dongguan City Guangdong, ChinaManufacturer0000api.fda.gov
Chiaphua Components (Jiangxi) LimitedYichun city Jiangxi, ChinaContract manufacturer0000api.fda.gov
Feishen Group CO., LTD.yongkang Zhejiang, ChinaContract manufacturer0000api.fda.gov
Guangdong Marshell Electric Vehicle CO., LTD.Zhaoqing Guangdong, ChinaContract manufacturer0000api.fda.gov
Hangzhou Rollmed Co.,ltd.Hangzhou Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Kunshan Hi-Fortune Health Products Co., Ltd.Kunshan City, Jiangsu, ChinaContract manufacturer0000api.fda.gov
Merits Healthcare Industries. (suzhou) Co., Ltd.Jiangsu Province, ChinaManufacturer0000api.fda.gov
Ningbo Gaobo Sports Co.,ltdNingbo Zhejiang, ChinaExporter to the US, Manufacturer, Repackager or relabeler0000api.fda.gov
Ningbo Ningyuan Import & Export Co., Ltd.Ningbo, Zhejiang, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Permobil (kunshan) Co., LtdKunshan Jiangsu, ChinaManufacturer0000api.fda.gov
Permobil Trading (kunshan) Co., LtdKunshan Jiangsu, ChinaContract manufacturer0000api.fda.gov
Viscount Hi-Tech (huizhou) Co., Ltd.Huizhou Guangdong, ChinaManufacturer0000api.fda.gov
Zhongshan Saxin Electric Heating Technology Co., Ltd.Zhongshan 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.