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Data / Medical devices / China / Dongguan Yijiaming Technology Co., Ltd.

Dongguan Yijiaming Technology Co., Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance

Dongguan Yijiaming Technology Co., Ltd. is registered with the FDA (registration 3043165181) in Dongguan Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 23, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3043165181
Address
Room 1502, Building T1, Dongguan Energy Zhengrun Digital Port, No.21 Qinyuan Road, Songshan Lake High-Tech Industrial Development Zone, Dongguan Guangdong, China, 523825
Owner or operator
Dongguan Yijiaming Technology Co., Ltd. (10094887)
Roles
Manufacturer
First device listed
December 31, 2025
Registered through
2026
Brand names listed
LED LIGHT THERAPY MASK (Model:HGMZ-2W-G1V1-EU,HGMZ-2W-G1V1-EU-06,HGMZ-2W-G1V1-YG), LED LIGHT THERAPY MASK (Model:HGMZ-2W-G2V1,RLTM-2DFACE-RV1,HGMZ-2W-G2V1-WHITE,HGMZ-2W-G2V1-PINK), LED LIGHT THERAPY MASK (Model:HGMZ-2W-G2V1-2,HGMZ-2W-G2V1-EU,HGMZ-2W-G2V1-WHITE-UK,HGMZ-2W-G2V1-UK), LED LIGHT THERAPY MASK (Model:HLGMZ-2W-G2V2), LED LIGHT THERAPY MASK (Model:HLGMZ-3W-G1V1,HLGMZ-3W-G2V1,HGMZ-2W-G1V1,HGMZ-2W-G2V1), LED LIGHT THERAPY MASK (Model:MRD-GJD-G3V1-BG,MRD-GJD-G3V1), LED LIGHT THERAPY MASK (Model:MRD-XJD-GJ-56LED,MRD-XJD-GJ-56LED-EU), LED LIGHT THERAPY MASK (Model:QCMZ-2W-G1V1,QCMZ-7+1BD-G1V1) and more

Devices it lists

DeviceProduct codeClassRoleSource
Light Based Over The Counter Wrinkle ReductionOHS2Manufactureraccessdata.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
December 23, 2025K253135LED Light Therapy Device (HLGMZ-3W-G1V1,HLGMZ-3W-G2V1,HLG-GJXJ-G1V1,HGMZ-2W-G1V1, HGMZ-2W-G2V1,MRD-GJXJ-G1V1.)OHSSubstantially EquivalentDongguan Yijiaming Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 23, 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.