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Data / Medical devices / China / Foshan Coxo Medical Instrument Co., Ltd.

Foshan Coxo Medical Instrument Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 7 510(k) clearances

Foshan Coxo Medical Instrument Co., Ltd. is registered with the FDA (registration 3014953747) in Foshan Guangdong, China. It lists 19 device types. The FDA files 7 510(k) clearances under its listings, the newest dated April 11, 2025. Registered through 2026. FDA data exported November 3, 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
3014953747
Address
No. 17, Guangming Ave., New Light Source Industrial Base, Nanhai National High-tech Zone, Foshan Guangdong, China, 528226
Owner or operator
Foshan COXO Medical Instrument Co., Ltd. (10075245)
Roles
Manufacturer
First device listed
June 10, 2020
Registered through
2026
Brand names listed
1002-21,1002-25,1002-31, 1003-21,1003-25,1003-31, 1004-21,1004-25,1004-31, 1202V-21,1202V-25,1202V-31, 1302-21,1302-25,1302-31, 1502-21,1502-25,1502-31, 1503-21,1503-25,1503-31, 1504-21,1504-25,1504-31 and more

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
April 11, 2025K243921LED Curing Lights (DB686 HALO)EBZSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
September 22, 2023K220179High-Speed Air Turbine Handpieces/Straight Handpieces/Geared Angle Handpieces/Air MotorsEFBSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
May 18, 2023K220829Endo MotorEKXSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
March 23, 2023K222096Endo Ultrasonic ActivatorELCSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
December 8, 2022K220826LED Curing LightEBZSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
September 27, 2022K220831Dental Implantation Systems, Dental Electrical MotorsEBWSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov
July 20, 2022K212178Root Apex LocatorLQYSubstantially EquivalentFoshan Coxo Medical Instrument Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 11, 2025. 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.