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Data / Medical devices / Staple, Implantable / China

FDA-registered makers of Staple, Implantable in China: 13 establishments

13 establishments in China are registered with the FDA to make Staple, Implantable (product code GDW). 12 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
Staple, Implantable
Product code
GDW
Country
China

Makers of Staple, Implantable in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medtronic (Shanghai) Medical Technology Co., Ltd.Min Hang District Shanghai, ChinaSpecification developer8November 30, 2022000api.fda.gov
Ezisurg Medical Co., Ltd.Shanghai, ChinaManufacturer5September 25, 2026000api.fda.gov
B.j.zh.f.panther Medical Equipment Co.,ltdBeijing, ChinaManufacturer3November 12, 2015000api.fda.gov
Fengh Medical Co., Ltd.Jiangyin Jiangsu, ChinaManufacturer3October 4, 2024000api.fda.gov
Ningbo Verykind Medical Device Co., Ltd.Ningbo Zhejiang, ChinaManufacturer2December 30, 2021000api.fda.gov
Touchstone International Medical Science Co., Ltd.Suzhou Jiangsu, ChinaManufacturer2September 26, 2014000api.fda.gov
Beijing Biosis Healing Biological Technology Co., LtdBeijing, ChinaManufacturer1May 27, 2021000api.fda.gov
Covidien Medical Products (Shanghai) Manufacturing LLCShanghai, ChinaManufacturer1December 8, 2000000api.fda.gov
Miconvey Technologies Co., Ltd.Chongqing, ChinaManufacturer1March 3, 2017000api.fda.gov
Reach Surgical, Inc.Tianjin, ChinaManufacturer1May 23, 2012000api.fda.gov
Sinolinks Medical Innovation, Inc.ChangZhou Jiangsu, ChinaManufacturer1July 5, 2013000api.fda.gov
Victor Medical Instruments Co., LtdChangzhou Jiangsu, ChinaManufacturer1December 5, 2016000api.fda.gov
Hangzhou Fushan Medical Appliance Co., Ltd.Hangzhou City Zhejiang, ChinaContract 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.