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Data / Medical devices / Injector And Syringe, Angiographic / China

FDA-registered makers of Injector And Syringe, Angiographic in China: 12 establishments

12 establishments in China are registered with the FDA to make Injector And Syringe, Angiographic (product code DXT). 8 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
Injector And Syringe, Angiographic
Product code
DXT
Country
China

Makers of Injector And Syringe, Angiographic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Shenzhen Boon Medical Supply Co., Ltd.Shenzhen Guangdong, ChinaManufacturer5August 22, 2024000api.fda.gov
Shandong Int Medical Instruments Co., LtdRizhao Shandong, ChinaManufacturer2September 5, 2025000api.fda.gov
Shenzhen Antmed Co. LtdDongguan Guangdong, ChinaManufacturer1May 2, 2008000api.fda.gov
Sunny Medical Device (shenzhen) Co., Ltd.Shenzhen Guangdong, ChinaContract manufacturer, Manufacturer1November 10, 2016000api.fda.gov
ShanDong WeiGao Group Medical Polymer Co., LtdWeihai Shandong, ChinaContract manufacturer, Contract sterilizer, Manufacturer1March 23, 2009000api.fda.gov
Union Medical Shenzhen Co., Ltd.Shenzhen Guangdong, ChinaManufacturer1December 12, 2017000api.fda.gov
Wuxi Yushou Medical Appliances Co., LtdWuxi City Jiangsu, ChinaManufacturer, Specification developer1November 22, 2016000api.fda.gov
Zhuhai DR Medical Instruments Co., Ltd.Zhuhai Guangdong, ChinaManufacturer1March 5, 2026000api.fda.gov
Changzhou DSB Medical Co., LtdChangzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Hangzhou Jincheng Medical Supplies Manufacture Co., Ltd.Hangzhou Zhejiang, ChinaContract manufacturer0000api.fda.gov
Jiangxi Baoeran Biomedical Science & Technology Co.,ltdFuzhou Jiangxi, ChinaContract manufacturer0000api.fda.gov
Vincent Medical (dong Guan) Manufacturing Co., Ltd.Dong Guan City Guangdong, ChinaContract manufacturer, Contract sterilizer0000api.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.