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Data / Medical devices / Tubing/Tubing With Filter, Insufflation, Laparoscopic / China

FDA-registered makers of Tubing/Tubing With Filter, Insufflation, Laparoscopic in China: 13 establishments

13 establishments in China are registered with the FDA to make Tubing/Tubing With Filter, Insufflation, Laparoscopic (product code NKC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Tubing/Tubing With Filter, Insufflation, Laparoscopic
Product code
NKC
Country
China

Makers of Tubing/Tubing With Filter, Insufflation, Laparoscopic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anhui Shiyin Photoelectric Instrument Co., Ltd.Suzhou Anhui, ChinaManufacturer, Specification developer0000api.fda.gov
Bio Protech Yantai IncYantai Shandong, ChinaManufacturer0000api.fda.gov
Changzhou Rongxin Medicine Minimal Invasion Technology Co., LtdJintan Jiangsu, ChinaManufacturer0000api.fda.gov
Diatrust Medical Co., Ltd.Nanjing City Jiangsu, ChinaManufacturer0000api.fda.gov
Gcmedica Enterprise Ltd.(wuxi)WUXI Jiangsu, ChinaContract manufacturer0000api.fda.gov
Gri Medical & Electronic Technology Co., Ltd.JIAXING Zhejiang, ChinaManufacturer0000api.fda.gov
Heng Chuang Plastic & Metal Co., LtdDongguan Guangdong, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
Smartdata Suzhou Co., LtdSuzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Suzhou Jingle Polymer Medical Apparatus Co., Ltd.SUZHOU Jiangsu, ChinaContract manufacturer0000api.fda.gov
Unimicro Medical Systems (shenzhen) Co., Ltd.ShenZhen Guangdong, ChinaManufacturer0000api.fda.gov
Xuzhou AKX Electronic Science and Technology Co., Ltd.Xuzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Yangzhou Fartley Medical Instrument Technology Co., LtdYangzhou Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Zhejiang Shuyou Surgical Instrument Co., LtdHuzhou Zhejiang, ChinaManufacturer0000api.fda.gov

Updated November 3, 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.