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Data / Medical devices / China / Sunglor Technology Co.,ltd

Sunglor Technology Co.,ltd: FDA-registered device maker in shenzhen Guangdong, China, 2 510(k) clearances

Sunglor Technology Co.,ltd is registered with the FDA (registration 3021282471) in shenzhen Guangdong, China. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 19, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021282471
Address
Rm. 306, 3nd Floor, Bldg. 4. Fuyong St.. Fuhai Science Technology Industrial Park Fuyong Community, Baoan Dist, shenzhen Guangdong, China, 518000
Owner or operator
SUNGLOR TECHNOLOGY CO.,LTD (10085580)
Roles
Manufacturer, Specification developer
First device listed
July 5, 2022
Registered through
2026
Brand names listed
LED Light Therapy Device (Model:SG-FSM, SG-NK, SG-CT), LED Light Therapy Device (Models: SG-FM, SG-FE), Led Light Therapy Device (SG-NK, SG-HD, SG-TW, SG-2700, SG-RM, SG-TC, SG-BB), Led Light Therapy Device (SG-TCPRO300, SG-TCPRO1000, SG-TCPRO1500, SG-MSK, SG-SL, SG-TRH), Red Light Therapy Device (SG-HS-FT, SG-WP, SG-AL, SG-MINI, SG-DP, SG-HT, SG-TP, SG-SW, SG-SLP)

Devices it lists

DeviceProduct codeClassRoleSource
Lamp, Infrared, Therapeutic HeatingILY2Manufacturer, Specification developeraccessdata.fda.gov
Light Based Over The Counter Wrinkle ReductionOHS2Manufacturer, Specification developeraccessdata.fda.gov
Over-The-Counter Powered Light Based Laser For AcneOLP2Manufacturer, Specification developeraccessdata.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 19, 2025K253086LED Light Therapy Device (Models: SG-FM, SG-FE)OHSSubstantially EquivalentSunglor Technology Co., Ltd.accessdata.fda.gov
November 19, 2025K253073LED Light Therapy Device (SG-FSM, SG-NK, SG-CT)OHSSubstantially EquivalentSunglor Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 19, 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.