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Data / Medical devices / Catheter, Straight / China

FDA-registered makers of Catheter, Straight in China: 15 establishments

15 establishments in China are registered with the FDA to make Catheter, Straight (product code EZD). 6 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
Catheter, Straight
Product code
EZD
Country
China

Makers of Catheter, Straight in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Chengdu Daxan Innovative Medical Tech. Co., Ltd.chengdu Sichuan, ChinaManufacturer2June 26, 2025000api.fda.gov
Hangzhou Jimushi Meditech Co., Ltd.Hangzhou Zhejiang, ChinaContract manufacturer, Manufacturer2June 24, 2026000api.fda.gov
Well Lead Medical Co. LtdGUANGZHOU Guangdong, ChinaContract manufacturer, Manufacturer2May 22, 2023000api.fda.gov
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaContract manufacturer, Manufacturer1August 21, 2009000api.fda.gov
Amsino Medical (shanghai) Co., Ltd.Shanghai, ChinaManufacturer1October 1, 2018000api.fda.gov
Coloplast (china) Ltd.ZHUHAI Guangdong, ChinaManufacturer1December 2, 2022000api.fda.gov
Conod Medical Shuyang Co., Ltd.Shuyang Jiangsu, ChinaContract manufacturer0000api.fda.gov
Conod Medical Co.,LimitedChangshu Jiangsu, ChinaContract manufacturer0000api.fda.gov
Haiyan Kangyuan Medical Instrument Co.,ltd.JiaXing Zhejiang, ChinaContract manufacturer0000api.fda.gov
Hangzhou Bever Medical Devices Co., Ltd.Hangzhou Zhejiang, ChinaSpecification developer0000api.fda.gov
Integral Medical Products Co., Ltd.SHAOXING Zhejiang, ChinaContract manufacturer0000api.fda.gov
Jiangsu Suyun Medical Materials Co., Ltd.Lianyungang Jiangsu, ChinaContract manufacturer0000api.fda.gov
Suzhou Jingle Polymer Medical Apparatus Co., Ltd.SUZHOU Jiangsu, ChinaContract manufacturer0000api.fda.gov
Shaoxing Fuqing Health Products Co., Ltd.Shaoxing Zhejiang, ChinaContract manufacturer0000api.fda.gov
Xianju Bever Medical Devices Co., Ltd.Taizhou 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.