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Data / Medical devices / China / Chongqing Jinshan Science & Technology (group) Co., Ltd

Chongqing Jinshan Science & Technology (group) Co., Ltd: FDA-registered device maker in Chongqing, China, 2 510(k) clearances

Chongqing Jinshan Science & Technology (group) Co., Ltd is registered with the FDA (registration 3011219572) in Chongqing, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 20, 2021. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3011219572
Address
No. 18, Nishang Road, Lianglu Industry City, Yubei District, Chongqing, China, 401120
Owner or operator
Chongqing Jinshan Science & Technology (Group) Co., Ltd (10047315)
Roles
Manufacturer
First device listed
August 7, 2014
Registered through
2026
Brand names listed
Disposable Impedance-pH catheter, Disposable Impedance-pH catheter/Disposable pH catheter, Disposable pH catheter, Endoscopic Irrigation Pump, Hysteroscopy System, Impedance-pH Reflux Monitoring Systems, pH Capsule Monitoring Systems

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 20, 2021K210618Beamer Aveo Irrigation Pump, Endolinq Endoscopic Irrigation Pump, Endoscopic Irrigation Pump SeriesOCXSubstantially EquivalentChongqing Jinshan Science & Technology Co., Ltd.accessdata.fda.gov
April 9, 2018K172151Hysteroscopy SystemHGHSubstantially EquivalentChongquin Jinshan Science & Technology (Group) Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 20, 2021. 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.