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Xiamen Ants Bro Technology Co., Ltd.: FDA-registered device maker in Xiamen City Fujian, China, 3 510(k) clearances

Xiamen Ants Bro Technology Co., Ltd. is registered with the FDA (registration 3016640651) in Xiamen City Fujian, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 29, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016640651
Address
No. 18 Xinyuan South Road, Haicang District, Xiamen City Fujian, China, 361026
Owner or operator
Xiamen Ants Bro Technology Co., Ltd. (10067284)
Roles
Exporter to the US, Manufacturer
First device listed
April 4, 2020
Registered through
2026
Brand names listed
Automatic Digital Blood Pressure Monitor, CHOSEN Infrared forehead thermometer, Digital thermometer, Infrared Forehead Thermometer, Marathon Automatic Digital Blood Pressure Monitor, Sigurd Automatic Digital Blood Pressure Monitor, VivaGuard HA-650 Infrared Forehead Thermometer, caring mill Infrared forehead thermometer and more

Devices it lists

DeviceProduct codeClassRoleSource
Continuous Measurement ThermometerFLL2Exporter to the US, Manufactureraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Exporter to the US, Manufactureraccessdata.fda.gov

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
May 29, 2020K190982Automatic Digital Blood Pressure MonitorDXNSubstantially EquivalentXiamen Ants Bro Technology Co., Ltd.accessdata.fda.gov
April 22, 2020K190984Infrared Forehead ThermometerFLLSubstantially EquivalentXiamen Ants Bro Technology Co., Ltd.accessdata.fda.gov
December 31, 2019K190990Digital ThermometerFLLSubstantially EquivalentXiamen Ants Bro Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 29, 2020. 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.