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Data / Medical devices / Analyzer, Body Composition / China

FDA-registered makers of Analyzer, Body Composition in China: 11 establishments

11 establishments in China are registered with the FDA to make Analyzer, Body Composition (product code MNW). 8 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
Analyzer, Body Composition
Product code
MNW
Country
China

Makers of Analyzer, Body Composition in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dongguan Tanita Health Equipment Co., Ltd.Dongguan City Guangdong, ChinaManufacturer4July 7, 2009000api.fda.gov
Shenzhen Healthcare Electronic Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer3June 28, 2012000api.fda.gov
Cha's Electronic Industries (shenzhen) Company LimitedShenzhen Guangdong, ChinaContract manufacturer, Manufacturer1May 12, 2009000api.fda.gov
Conmo Electronic Company LimitedHuizhou City Guangdong, ChinaContract manufacturer, Manufacturer1May 30, 2014000api.fda.gov
Shenzhen BelterHealthMeasurementAndAnalysisTechnologyCo.,LtdShenzhen Guangdong, ChinaManufacturer1January 4, 2013000api.fda.gov
Shenzhen Shine Industrial Co., Ltd.Shenzhen Guangdong, ChinaManufacturer1April 9, 2012000api.fda.gov
Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.Zhongshan Guangdong, ChinaManufacturer1June 15, 2024000api.fda.gov
Zhongshan Transtek Electronics Co., LtdZhongshan Guangdong, ChinaContract manufacturer, Manufacturer1May 30, 2013000api.fda.gov
Andon Health Co., LtdTianjin, ChinaManufacturer0000api.fda.gov
Krell Precision (yangzhou) Co., LtdYANGZHOU Jiangsu, ChinaContract manufacturer0000api.fda.gov
Measurement Ltd.Kowloon City, ChinaContract 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.