SUNGROW TECHNOLOGY CO.,LIMITED

FDA Device Registration & Listing · HONG KONG, CN · Registration 3033883954

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
3033883954
FEI Number
3033883954
Entity Name
SUNGROW TECHNOLOGY CO.,LIMITED
City/State/Country
HONG KONG, CN
Establishment Address
No.185 G/F, HANG WAI IND.CENTRE, NO.6 KIN TAI ST., TUEN MUN, N.T, HONG KONG 999077, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Sungrow Technology Co.,Limited (Owner Number: 10091832)
Owner / Operator Contact Address
No.185 G/F, HANG WAI IND.CENTRE, NO.6 KIN TAI ST., TUEN MUN, N.T, HONG KONG, CN-NOTA 999077, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Belt, Red Light Belt, LED Red Light Belt, LED Light Mat: (BE-G122, BE-G66, BE-G56, BE-G80, G56, BE120, BE120P, BE105P, PC03, PC04); BE105, BE405, BE150, L01, L02, L03, L04, L05, L06, D01, D02, D03, D04, D05, D06, BE400, BE700, BE400, BE700, PC01, PC02, Pad, Mat, PEMF Mat, Heating Mat: (PE01, PE02, PE03, PE04) A1200, E300, E600, E900, E1500, E1800, E2400, E4500, MAX300, MAX900, MAX1800, MAX4800, MINI60PRO, MATEPRO75, PRO200, G66, G120, G260, G280, G288, G300, G360, G480, G1280, G1980, G2030, G3040, G3060) LED Silicone Mask (G06, G10, G11, G11P, G12, G13, G14, G15, G15P, G15K, G16, G17, G18, G19, G20, G11V2, G240, G56, P40A, P40B, P40MAX, BK200, BK300, BK900, BK1800, MINI60S, SPRO200, SPRO300, MZ01, MZ02, S009-001, S009-002, S009-003, LED Therapy Light: (ESPLUS360, ESPLUS750, ESPLUS1500, ESPLUS4500, ESPLUS5400, SL280, S300, S750, S1500, A300, A600, TBZ104, MINI60S); Beauty Device (MY01, MY02, MY24, MS01, MS02, MS03, MS04, C01, C02, C03, HC03, HC04, T01, T02, T03, T04, HG02, HG03, HG04, HG06)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRT Pad, Heating, Powered Physical Medicine Class 2 890.5740 2024-11-06
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-11-06
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-11-06

Official Correspondent

YAFEN ZHANG

US Agent Details

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

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881862 Thermo Body Wrap Systems, Inc. THERMO-BODY-WRAP SYSTEM 1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033883954. Last updated year: 2026. Please use registration number 3033883954 when referencing this establishment in official correspondence.
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