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Data / Medical devices / Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use / China

FDA-registered makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use in China: 12 establishments

12 establishments in China are registered with the FDA to make Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use (product code PYO). 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
Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use
Product code
PYO
Country
China

Makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anji Huayong Biotech Co LtdGui Shan Town Zhejiang, ChinaManufacturer0000api.fda.gov
Fesun Shanghai Co., Ltd.shanghai, ChinaExporter to the US, Manufacturer0000api.fda.gov
Hynaut Health Technology Co., LTD.Qingdao Shandong, ChinaManufacturer0000api.fda.gov
Jiangsu Qiantai Medical Instrument Co., Ltd.Tai zhou Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Jinhua Jingdi Medical Supplies Co.,ltdJinhua Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
JM Medical Co., Ltd.Liaocheng Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Nanning Sixtant Biotechnology Co., LtdNanning Guangxi, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shanghai Lions Industrial Co.,ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Shanghai Jolly Industrial Co., Ltd.Shanghai, ChinaContract manufacturer, Exporter to the US0000api.fda.gov
Wuhan Sitaili Medical Apparatus Development Co.,ltdWuhan Hubei, ChinaManufacturer0000api.fda.gov
Weihai Kangzheng Medical Equipments Technology Co.,Ltdweihai Shandong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhejiang Hongyu Medical Commodity Co., Ltd.YIWU Zhejiang, ChinaContract manufacturer, Exporter 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.