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Data / Medical devices / China / Shenzhen Sungrow Led Technology Co.,ltd

Shenzhen Sungrow Led Technology Co.,ltd: FDA-registered device maker in shenzhen Guangdong, China, 1 510(k) clearance

Shenzhen Sungrow Led Technology Co.,ltd is registered with the FDA (registration 3016171836) in shenzhen Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 9, 2025. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3016171836
Address
3F, 2# Factory Bldg (Phase I), Bangkai Sci & Tech Ind Park, Guangming High-Tech Ind Park, shenzhen Guangdong, China, 518132
Owner or operator
Shenzhen Sungrow LED Technology Co.,LTD (10061584)
Roles
Exporter to the US, Manufacturer
First device listed
October 31, 2019
Registered through
2026
Brand names listed
2-2040, 4-54, 4-360, 4-720, 4-1020, 4-2040, 5-54, 5-560, 5-1040, 5-1440, 5-2520, 5-6120, LP-RJVGLW-WHT, LumaGlow,, BK300, BK900, BK1800, MINI60S, SPRO200, SPRO300, MZ01, MZ02, S009-001, S009-002, S009-003, BlockBlueLight MINI,, Beauty Device (MY01, MY02, MY24, MS01, MS02, MS03, MS04, C01, C02, C03, HC03, HC04, T01, T02, T03, T04, HG02, HG03,, Belt, Red Light Belt, LED Red Light Belt, LED Light Mat: (BE-G122, BE120, BE120P, BE105P, BE105, BE405, BE150, L01, L02,, BlockBlueLight MEGA, BlockBlueLight ELITE XL, BlockBlueLight ULTIMATE XXL, BlockBlueLight MEGA PLUS, MitoPRO X series,, BlockBlueLight PORTABLE, BlockBlueLight TABLETOP, BlockBlueLight MID, BlockBlueLight PRO, BlockBlueLight MAX,, E1500, E1800, E2400, E4500, MAX300, MAX900, MAX1800, MAX4800, MINI60PRO, MATEPRO75, PRO200, P40A, P40B, P40MAX, BK200,, ESPLUS360, ESPLUS750, ESPLUS1500, ESPLUS4500, ESPLUS5400, SL280, S300, S750, S1500, A300, A600, A1200, E300, E600, E900, 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 9, 2025K250830LED Light Therapy Mask (G15, G15P, G15K, G11P, G11, G10, G13, G14, G17, VISO, PRANA, Chin2Chest, BBL-FACEMASK)OHSSubstantially EquivalentShenzhen Sungrow Led Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 9, 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.