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Data / Medical devices / Strip, Temperature, Forehead, Liquid Crystal / China

FDA-registered makers of Strip, Temperature, Forehead, Liquid Crystal in China: 9 establishments

9 establishments in China are registered with the FDA to make Strip, Temperature, Forehead, Liquid Crystal (product code KPD). 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
Strip, Temperature, Forehead, Liquid Crystal
Product code
KPD
Country
China

Makers of Strip, Temperature, Forehead, Liquid Crystal in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Chants (foshan) Technology Co.,ltdFoshan Guangdong, ChinaExporter to the US, Manufacturer, Repackager or relabeler0000api.fda.gov
Dongguan E-Test Technology Co.,ltdDongguan Guangdong, ChinaComplaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler0000api.fda.gov
Dongyang City Yonoel Outdoor Products Co.,ltdDongyang Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Guangdong Dexin Sports Industry Co.,ltdGuangzhou Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer0000api.fda.gov
Ningbo Tianbo First Aid Product Co., Ltd.Ningbo Zhejiang, ChinaManufacturer0000api.fda.gov
Planet (anhui) Medical Products Co., LtdChuzhou Anhui, ChinaContract manufacturer0000api.fda.gov
Saferlife Products Co.,ltd.Guangzhou Guangdong, ChinaManufacturer, Repackager or relabeler0000api.fda.gov
Shenzhen Joose Beauty Electronic Co.,ltdShen Zhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer0000api.fda.gov
Suzhou Pulikang Medical Device Co LtdSuzhou Jiangsu, ChinaExporter to the US, 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.