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Data / Medical devices / Trocar / China

FDA-registered makers of Trocar in China: 8 establishments

8 establishments in China are registered with the FDA to make Trocar (product code DRC). 2 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
Trocar
Product code
DRC
Country
China

Makers of Trocar in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Shanghai Microport Ep Medtech Co., Ltd.Shanghai, ChinaManufacturer1March 23, 2022000api.fda.gov
Synaptic Medical LimitedBeijing, ChinaManufacturer1August 29, 2014000api.fda.gov
Boen Healthcare Co., Ltd.Suzhou Jiangsu, ChinaExporter to the US, Specification developer0000api.fda.gov
Changzhou 3R Medical Device Technology Co., Ltd.Changzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Changzhou Lookmed Medical Instrument Co.,ltdChangzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Sunny Medical Device (shenzhen) Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shanghai INT Medical Instruments Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Tianck Medical Co.,ltdHuizhou Guangdong, 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.