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Data / Medical devices / Shield, Nipple / China

FDA-registered makers of Shield, Nipple in China: 15 establishments

15 establishments in China are registered with the FDA to make Shield, Nipple (product code HFS). 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
Shield, Nipple
Product code
HFS
Country
China

Makers of Shield, Nipple in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaContract manufacturer0000api.fda.gov
B&a Precision Silicone Rubber (dongguan) Co., LtdDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Changzhou Dailys Care Products Co.,ltd.Changzhou Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Essentia Industries Ltd.Dong Guan Guangdong, ChinaManufacturer0000api.fda.gov
Fansheng Technology (guangdong) Co., Ltd.Zhongshan City Guangdong, ChinaContract manufacturer0000api.fda.gov
Health Plus (shanghai) International Co., LtdShanghai, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Infinique Electronic (dongguan) Co. Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Jiangsu Senwo Medical Technology Co., Ltd.Nantong Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Jiangxi Partner Home Co., Ltd.Nanchang City Jiangxi, ChinaExporter to the US, Manufacturer0000api.fda.gov
Linhejiacheng (shenzhen) E-Commerce Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Ningbo Just Soon Industrial LimitedNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
Ninghai Shengyue Electrical Appliance Co.,ltdNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
RrdonnelleyDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Root Innovation Technology Co., Ltd.Shenzhen Guangdong, ChinaSpecification developer0000api.fda.gov
Zhejiang Jinhua Huatong Medical Appliance Co., Ltd.Jinhua Zhejiang, 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.