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Data / Medical devices / Enteral Syringes With Enteral Specific Connectors / China

FDA-registered makers of Enteral Syringes With Enteral Specific Connectors in China: 12 establishments

12 establishments in China are registered with the FDA to make Enteral Syringes With Enteral Specific Connectors (product code PNR). 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
Enteral Syringes With Enteral Specific Connectors
Product code
PNR
Country
China

Makers of Enteral Syringes With Enteral Specific Connectors in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Shantou Wealy Medical Instrument Co., Ltd.SHANTOU Guangdong, ChinaManufacturer2August 27, 2021000api.fda.gov
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaManufacturer1March 30, 2018000api.fda.gov
Jiangsu Caina Medical Co., LtdJiangyin Jiangsu, ChinaContract manufacturer, Manufacturer1August 6, 2019000api.fda.gov
Jiangsu Kangbao Medical Equipment Co., LtdYangzhou Jiangsu, ChinaContract manufacturer, Manufacturer1November 9, 2018000api.fda.gov
Jiangsu Micsafe Medical Technology Co., LtdYancheng Jiangsu, ChinaManufacturer1October 11, 2018000api.fda.gov
Ningbo Tianyi Medical Appliance CO., Ltd.Ningbo Zhejiang, ChinaContract manufacturer, Contract sterilizer, Manufacturer1April 28, 2021000api.fda.gov
Shandong Ande Healthcare Apparatus Co., Ltd.Zibo Shandong, ChinaManufacturer1September 12, 2020000api.fda.gov
VR Medical Technology Co., Ltd.KUNSHAN Jiangsu, ChinaManufacturer1September 22, 2016000api.fda.gov
Aena Medical (jiangsu) Co.,ltd.Jiangyin City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Amsino Medical (shanghai) Co., Ltd.Shanghai, ChinaContract manufacturer0000api.fda.gov
Anhui Tiankang Medical Technology Co., Ltd.Tianchang Anhui, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.Chengdu Sichuan, 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.