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Data / Medical devices / China / Shenzhen Brav Electronic Technologies Co., Ltd

Shenzhen Brav Electronic Technologies Co., Ltd: FDA-registered device maker in shenzhen Guangdong, China, 2 510(k) clearances

Shenzhen Brav Electronic Technologies Co., Ltd is registered with the FDA (registration 3008975047) in shenzhen Guangdong, China. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 1, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3008975047
Address
4-5/F, Block 11, Tongfuyu Industrial District, Lezhujiao, Huangmabu Community, Xixiang, Baoan,Shenzhen., shenzhen Guangdong, China, 518102
Owner or operator
ShenZhen BRAV Electronic Technologies Co., Ltd. (10057455)
Roles
Contract manufacturer, Manufacturer
First device listed
April 17, 2018
Registered through
2026
Brand names listed
Elecrtronic Blood Pressure Monitor, Model: BP-201, BP-202, BP-203, BP-204, BP-205, BP-206, Infrared Thermometer MODEL:EFT-161,EFT-162,EFT-163,EFT-164,EFT-165,EFT-166, Water Flosser BV-609, BV-608, BV-212, BV-208, BV-210, BV-610, BV-611,BV-612,BV-520

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 1, 2026K260470Electronic Blood Pressure Monitor (BP-204C, BP-204A, BP-215, BP-203C, BP-205A, BP-201C, BP-217, BP-202C, BP-202 BP-205, BP-205B,BP-206)DXNSubstantially EquivalentShenzhen Brav Electronic Technologies Co., Ltd.accessdata.fda.gov
March 2, 2018K171214Infrared ThermometerFLLSubstantially EquivalentShenzhen Brav Electronic Technologies Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 1, 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.