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Data / Medical devices / Monitor, Bed Patient / China

FDA-registered makers of Monitor, Bed Patient in China: 15 establishments

15 establishments in China are registered with the FDA to make Monitor, Bed Patient (product code KMI). 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
Monitor, Bed Patient
Product code
KMI
Country
China

Makers of Monitor, Bed Patient in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ari Medical Technology Co., Ltd.Hefei Anhui, ChinaManufacturer0000api.fda.gov
Chengdu Li Ren Electric Co., LtdChengdu Sichuan, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Fastsound Acoustic Technology (hangzhou) Co., Ltd.Hangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Foshan Fuzikon Medical Technology Co.LtdFoshan Guangdong, ChinaManufacturer0000api.fda.gov
Hebei Healthplus Medical Device Co LtdHandan city Hebei, ChinaManufacturer0000api.fda.gov
Jiangsu Rooe Medical Technology Co., Ltd.Zhangjiagang City Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Perth Electronic Plastic Limited CompanyDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Giftshine Technology Co LtdSHENZHEN Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Shenzhen Shengzhou Intelligent Equipment R&D Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Contin Medical Device Co., Ltd.Shenzhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Suzhou Meccan Import and Export Corp.Suzhou Jiangsu, ChinaContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Xiamen Sheep Anti Fatigue Mat Co LtdXiamen City Fujian, ChinaManufacturer0000api.fda.gov
Yingkou Henyi Flow Control Inc.Yingkou City Liaoning, ChinaManufacturer0000api.fda.gov
Yuiyn Hoo Industrial LimitedDong Guan City Guangdong, ChinaContract manufacturer0000api.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.