SHENZHEN SUNGROW LED TECHNOLOGY CO.,LTD

FDA Device Registration & Listing · shenzhen Guangdong, CN · Registration 3016171836

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016171836
FEI Number
3016171836
Entity Name
SHENZHEN SUNGROW LED TECHNOLOGY CO.,LTD
City/State/Country
shenzhen Guangdong, CN
Establishment Address
3F, 2# Factory Bldg (Phase I), Bangkai Sci & Tech Ind Park, Guangming High-Tech Ind Park, shenzhen Guangdong 518132, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Shenzhen Sungrow LED Technology Co.,LTD (Owner Number: 10061584)
Owner / Operator Contact Address
3F, 2# Factory Bldg (Phase I), Bangkai Sci & Tech Ind Park, Guangming High-Tech Ind Park, Shenzhen, CN-GD 518132, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Eye Mask (EM01, EM02, EM03, EM04, EM05, EP01, EP02, LP01, LP02) BlockBlueLight MEGA, BlockBlueLight ELITE XL, BlockBlueLight ULTIMATE XXL, BlockBlueLight MEGA PLUS, MitoPRO X series, BlockBlueLight PORTABLE, BlockBlueLight TABLETOP, BlockBlueLight MID, BlockBlueLight PRO, BlockBlueLight MAX, G16, G17, G18, G19, G20, G11V2, G240, G56, G66, G120, G260, G280, G288, G300, G360, G480, G1280, G1980, G2030, G3040, G3060, Combo Mask, BBL-FACEMASK, VISO, PRANA, ChinChest, SP01 LumaGlow Duo, LumaGlow Computer Light Bar, X 1500w, S 300w, MINI, G06, G10, G11, G11P, G12, G13, G14, G15, G15P, G15K, MitoPRO 300X, MitoPRO 750X, MitoPRO 1500X, MitoPRO MEGAX, MitoPRO ELITEX, MitoPRO ULTIMATEX, PRO300, PRO750, PRO1500, ESPLUS360, ESPLUS750, ESPLUS1500, ESPLUS4500, ESPLUS5400, SL280, S300, S750, S1500, A300, A600, A1200, E300, E600, E900, PRO4500, HG200, HG300, HG500, HG1000, HG1500, ULTRA360, ULTRA750, ULTRA1500, ULTTRA4500, 2-54, 2-360, 2-720, 2-1020, E1500, E1800, E2400, E4500, MAX300, MAX900, MAX1800, MAX4800, MINI60PRO, MATEPRO75, PRO200, P40A, P40B, P40MAX, BK200, 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, HG04, HG06) Beauty Device (MY01, MY02, MY24, MS01, MS02, MS03, MS04, C01, C02, C03, HC03, HC04, T01, T02, T03, T04, HG02, HG03, LED Light Therapy Mask (models: G15, G15P, G15K, G11P, G11, G10, G13, G14, G17, VISO, PRANA, Chin2Chest, BBL-FACEMASK)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2019-10-31
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2019-10-31
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-10-20
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2025-06-13
OLP Over-The-Counter Powered Light Based Laser For Acne General, Plastic Surgery Class 2 878.4810 2025-06-13

Official Correspondent

SenHua Liu

US Agent Details

Yafen Zhang Business: Purelux Tech INC Email: info@pureluxtech.com Phone: (949) 8166662

Related Public Records

Same Entity

Shenzhen Sungrow LED Technology Co.,LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016171836. Last updated year: 2026. Please use registration number 3016171836 when referencing this establishment in official correspondence.
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