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Data / Medical devices / Collector, Ostomy / China

FDA-registered makers of Collector, Ostomy in China: 15 establishments

15 establishments in China are registered with the FDA to make Collector, Ostomy (product code EXB). 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
Collector, Ostomy
Product code
EXB
Country
China

Makers of Collector, Ostomy in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aimi Health Technology (Guangdong) Co., Ltd.Dongguan City Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Boen Healthcare Co., Ltd.Suzhou Jiangsu, ChinaExporter to the US, Specification developer0000api.fda.gov
Coloplast (china) Ltd.ZHUHAI Guangdong, ChinaManufacturer0000api.fda.gov
Concarey Medical Technology Co., LtdShanghai, ChinaExporter to the US, Manufacturer0000api.fda.gov
Dongguan Hong De Medical Plastic Products Co. Ltd.Dongguan Guangdong, ChinaManufacturer0000api.fda.gov
Hangzhou Rollmed Co.,ltd.Hangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Hubei Hendry Medical Appliance Co., LtdXiaogan City Hubei, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiangsu Ostup Medical Products Co. Ltd.Nanjing Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Nanjing Anjian Medical Device Co.,ltd.Nanjing Jiangsu, ChinaContract manufacturer0000api.fda.gov
Shanghai Lions Industrial Co.,ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Shaoxing Haoshide Medical Products Co.,ltdShaoxing Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Suzhou Kangyouwei Medical Technology Co., Ltd.Suzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Shanghai Jolly Industrial Co., Ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Tongxiang Bao-Health Medical Instrument Co., Ltd.Tongxiang Zhejiang, ChinaManufacturer0000api.fda.gov
Wenzhou Zuoyou Medical Technoloyg Co.,ltd.Wenzhou Zhejiang, ChinaContract manufacturer, Exporter 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.