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Data / Medical devices / Support, Breathing Tube / China

FDA-registered makers of Support, Breathing Tube in China: 13 establishments

13 establishments in China are registered with the FDA to make Support, Breathing Tube (product code JAY). 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
Support, Breathing Tube
Product code
JAY
Country
China

Makers of Support, Breathing Tube in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Dongguan Shihui Living Products Ltd.Dongguan Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Dongguan Vincent Rehab Devices Company LimitedDONGGUAN Guangdong, ChinaContract manufacturer0000api.fda.gov
IPE Plastic & Hardware Industy, LTDDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Jan Mao Industries Co., Ltd.Guangxi Zhuang Autonomous Region, ChinaExporter to the US, Manufacturer0000api.fda.gov
Lingxian Dongsheng Textile Co., Ltd.Dezhou Shandong, ChinaManufacturer0000api.fda.gov
Ningbo Castle Medical Import & Export Co.,ltdNingbo Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Ningbo Chibanda Imp &exp Co, LtdNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
Ningbo Huakun Medical Equipment Co.,ltdCixi Zhejiang, ChinaManufacturer0000api.fda.gov
Resvent Medical Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shandong Zhushi Pharmaceutical Group Co., LtdHeze Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shaoxing Haitech Medical Products Co., LtdSHAOXING Zhejiang, ChinaManufacturer0000api.fda.gov
Suzhou Avon Textile Co., Ltd.Suzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Suzhou Shangchuang Technology Service Co., Ltd.Suzhou Jiangsu, 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.