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Data / Medical devices / China / Foshan Guangyu Weilai Medical Equipment Co., Ltd.

Foshan Guangyu Weilai Medical Equipment Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance

Foshan Guangyu Weilai Medical Equipment Co., Ltd. is registered with the FDA (registration 3039443706) in Foshan Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 20, 2025. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3039443706
Address
201, Block A, Zhongfa Zhaochuang Science and Technology Park, River Village, Lishui Town, Nanhai District, Foshan Guangdong, China, 528226
Owner or operator
Foshan Guangyu Weilai Medical Equipment Co., Ltd. (10093755)
Roles
Manufacturer
First device listed
July 2, 2025
Registered through
2026
Brand names listed
Body Massager Machine (Model: MLX-3999,MLX-3999-41), LED LIGHT MASK (A093), LED LIGHT MASK (A097-C,A097-A), LED LIGHT THERAPY MASK(Model:A097-A-SAPPHIRE,A097-A-ROSEGOLD,A097-C-SAPPHIRE ,A097-C-ROSEGOLD), LED Light Therapy Panel ( Model:A081/A083), LED Light Therapy Panel(Model:A081-US,A081-EU,A081-UK), LED Light Therapy Panel(Model:A083-J-US,A083-J-EU,A083-J-UK), LED Light Therapy Panel(Model:A083-SUN-US,A083-SUN-EU,A083-SUN-UK) 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
June 20, 2025K250880LED LIGHT MASK (A093)OHSSubstantially EquivalentFoshan Guangyu Weilai Medical Equipment Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 20, 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.