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Data / Medical devices / Mixer, Cement, For Clinical Use / China

FDA-registered makers of Mixer, Cement, For Clinical Use in China: 12 establishments

12 establishments in China are registered with the FDA to make Mixer, Cement, For Clinical Use (product code JDZ). 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
Mixer, Cement, For Clinical Use
Product code
JDZ
Country
China

Makers of Mixer, Cement, For Clinical Use in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beijing ZKSK Technology Co., Ltd.beijing, ChinaManufacturer0000api.fda.gov
CDM Center Of Excellence Ltd.Beijing, ChinaManufacturer0000api.fda.gov
Debo Medical Technology (shijiazhuang) Co., Ltd.Shijiazhuang Hebei, ChinaContract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer, Repackager or relabeler0000api.fda.gov
Dongguan Kaiser Technology Co., LtdDongguan city Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Guangzhou Clean Medical Products Manufacturing CorpGuangzhou Guangdong, ChinaComplaint file establishment, Manufacturer0000api.fda.gov
Hubei Guarddent Medical Technology Co.,ltdWuhan Hubei, ChinaExporter to the US, Manufacturer0000api.fda.gov
Huizhou Videya Technology Co., Ltd.Huizhou Guangdong, ChinaManufacturer0000api.fda.gov
Hicren (Zhejiang) Medtech Co., Ltd.Ningbo Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jie Gao Plastic Products Co., Ltd.DONGGUAN CITY Guangdong, ChinaContract manufacturer0000api.fda.gov
Premium Plus (dongguan) LimitedDongguan Guangdong, ChinaManufacturer0000api.fda.gov
Suzhou Pac-Dent Technology Co., LtdSUZHOU CITY Jiangsu, ChinaManufacturer0000api.fda.gov
Tangshan Zhengtong Exhibition Co., Ltd.Tangshan Hebei, 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.