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Data / Medical devices / Tip, Rubber, Oral Hygiene / China

FDA-registered makers of Tip, Rubber, Oral Hygiene in China: 15 establishments

15 establishments in China are registered with the FDA to make Tip, Rubber, Oral Hygiene (product code JEW). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Tip, Rubber, Oral Hygiene
Product code
JEW
Country
China

Makers of Tip, Rubber, Oral Hygiene in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CDM Center Of Excellence Ltd.Beijing, ChinaManufacturer0000api.fda.gov
Essentia Industries Ltd.Dong Guan Guangdong, ChinaManufacturer0000api.fda.gov
Guang Xi Fulaiming Biopharmaceutics Co., Ltd.Nanning Guangxi, ChinaManufacturer0000api.fda.gov
Guangzhou Four E's Scientific Co., Ltd.GUANGZHOU Guangdong, ChinaSpecification developer0000api.fda.gov
Huanghua DK Dental Co., LtdHuangHua Hebei, ChinaManufacturer0000api.fda.gov
Jiangmen Zhi Qu Metal Plastic Industrial Co., Ltd.Jiangmen, Guangdong, ChinaManufacturer0000api.fda.gov
Jiangsu Zhong Heng Pet Articles Joint-Stock Co.,ltdYancheng Jiangsu, ChinaManufacturer0000api.fda.gov
Jiangxi Partner Home Co., Ltd.Nanchang City Jiangxi, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jinyuan Medical Equipment(tianjin)co.,ltdTianjin, ChinaManufacturer0000api.fda.gov
Ningbo Aolbea Oral Care Products Co., LtdYuyao City Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Qibei Technology Co., LimitedKL Hong Kong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Sino-Vista Dental Instruments Co., Ltd.Zibo Shandong, ChinaContract manufacturer0000api.fda.gov
Suzhou Fumaite Oral Care Products Co. Ltd.Suzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Xingyue Medical Health Technology (nanjing) Co., Ltd.Nanjing Jiangsu, ChinaManufacturer0000api.fda.gov
Zhejiang Lidesen Medical Instrument Co., LtdHangzhou Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated November 3, 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.