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Data / Medical devices / Cover, Barrier, Protective / China

FDA-registered makers of Cover, Barrier, Protective in China: 13 establishments

13 establishments in China are registered with the FDA to make Cover, Barrier, Protective (product code MMP). 3 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
Cover, Barrier, Protective
Product code
MMP
Country
China

Makers of Cover, Barrier, Protective in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Premier Guard Zhongshan LimitedZhongshan Guangdong, ChinaManufacturer1November 30, 2004000api.fda.gov
Shanghai Huayue Packaging Products Co., Ltd.Fengxian District, Shanghai, ChinaContract manufacturer, Manufacturer1February 19, 2002000api.fda.gov
Shanghai Leyi Plastic Products Co LtdShanghai, ChinaContract manufacturer, Manufacturer1February 19, 2002000api.fda.gov
Changzhou DSB Medical Co., LtdChangzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Dongguan Shin Yi Healthcare Products FactoryDONG GUAN CITY Guangdong, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
Dongguan Hong De Medical Plastic Products Co. Ltd.Dongguan Guangdong, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
Dongguan SafeSecure Plastics Co., Ltd.Dongguan City Guangdong, ChinaContract manufacturer0000api.fda.gov
Heyuan Hong De Medical Products Co., Ltd.Heyuan City Guangdong, ChinaContract manufacturer0000api.fda.gov
Principle & Will Biotech (Pinghu) Co., Ltd.Pinghu City Zhejiang, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
S.E.S. Healthcare Products Co., Ltd.Heifei Anhui, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
S.E.S. Healthcare Products Co., Ltd.Huainan City Anhui, ChinaContract manufacturer0000api.fda.gov
Sino Protection (Hefei) Medical Products Co. ltd.HEFEI Anhui, ChinaContract manufacturer0000api.fda.gov
Suzhou Pac-Dent Technology Co., LtdSUZHOU CITY Jiangsu, 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.