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Shenzhen Borria Technology Co.,ltd: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances

Shenzhen Borria Technology Co.,ltd is registered with the FDA (registration 3021599225) in Shenzhen Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 7, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021599225
Address
Room 601, Building 24, Shatoujiao Industrial Zone, Yantian Comprehensive Bonded Zone, No. 2015 Shenyan Road, Shenzhen Guangdong, China, 518081
Owner or operator
SHENZHEN BORRIA TECHNOLOGY CO.,LTD (10083846)
Roles
Manufacturer
First device listed
December 22, 2021
Registered through
2026
Brand names listed
5 in 1 Led Light Therapy Panel (Model: F5), Facial Beauty Device(Model: M4), IPL Hair Removal Device: BR223, BR225, IPL Hair Removal Machine:BR2020/ Hyper Sunk Technologies (Ipl Laser Hair Removal Machines), LED Beauty Instrument(M2, M2 Pro, BR-068), LED EYE MASK (Model: M6), LED FACIAL MASK(M226, M226-A, F2,), LED Face & Neck Therapy Mask (Model: MN7) 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 7, 2025K242385LED Therapy Mask (MN1, M226)OHSSubstantially EquivalentShenzhen Borria Technology Co., Ltd.accessdata.fda.gov
December 15, 2023K232939IPL Hair Removal DeviceOHTSubstantially EquivalentShenzhen Borria Technology Co., Ltd.accessdata.fda.gov
December 16, 2021K213020IPL hair removal machineOHTSubstantially EquivalentShenzhen Borria Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 7, 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.