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Data / Medical devices / Strip, Adhesive, Closure, Skin / China

FDA-registered makers of Strip, Adhesive, Closure, Skin in China: 13 establishments

13 establishments in China are registered with the FDA to make Strip, Adhesive, Closure, Skin (product code FPX). 1 has 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
Strip, Adhesive, Closure, Skin
Product code
FPX
Country
China

Makers of Strip, Adhesive, Closure, Skin in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Rfx+care Manufacturing Co., Ltd.Shaoxing Zhejiang, ChinaExporter to the US, Manufacturer, Repackager or relabeler1July 14, 1993000api.fda.gov
Boen Healthcare Co., Ltd.Suzhou Jiangsu, ChinaExporter to the US, Specification developer0000api.fda.gov
Derma Sciences Nantong IncorporationDEVELOPMENT Jiangsu, ChinaContract manufacturer0000api.fda.gov
HongYu BioTech (ShenZhen) Co., LtdShenzhen Guangdong, ChinaContract manufacturer, Exporter to the US0000api.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, Exporter to the US, Manufacturer0000api.fda.gov
Jiujiang Jiebao Medicine Equipment Co., LtdJiujiang City Jiangxi, ChinaExporter to the US, Manufacturer0000api.fda.gov
Qidong Farjoy Medical Material Co., Ltd.Qidong Jiangsu, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Yafho Bio-Technology Co., Ltd.GUANGZHOU Guangdong, ChinaManufacturer0000api.fda.gov
Yiwu Haoding Medical Co.,ltdYiwu Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Zhejiang Hangbiao Medical Products Co.,ltdJinhua Zhejiang, ChinaManufacturer0000api.fda.gov
Zhejiang Haomep Medical Products Co.,ltdYIWU Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhejiang Longterm Medical Technology Co., LTDHuzhou City 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.