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Data / Medical devices / Climber, Curb, Wheelchair / China

FDA-registered makers of Climber, Curb, Wheelchair in China: 13 establishments

13 establishments in China are registered with the FDA to make Climber, Curb, Wheelchair (product code IMN). 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
Climber, Curb, Wheelchair
Product code
IMN
Country
China

Makers of Climber, Curb, Wheelchair in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
China Wonderland Nurserygoods Co., Ltd.Dongguan City Guangdong, ChinaManufacturer0000api.fda.gov
Cradle Medical Equipment Technology Co.ltdFoshan Guangdong, ChinaManufacturer0000api.fda.gov
Chiaphua Components (Jiangxi) LimitedYichun city Jiangxi, ChinaContract manufacturer0000api.fda.gov
Dragon Medical Co.,LtdSuzhou City Jiangsu, ChinaManufacturer0000api.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
Permobil (kunshan) Co., LtdKunshan Jiangsu, ChinaManufacturer0000api.fda.gov
Quality Life Technologies Co., Ltd.Dongguan Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Trolli King (holding) Ltd.Shenzhen Guangdong, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Yang-Tze Healthcare Products Co, LimitedDongguan 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.