GUANGDONG FUQIANG BEAUTY EQUIPMENT CO.,LIMITED

FDA Device Registration & Listing · Qingyuan Guangdong, CN · Registration 3043140693

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
3043140693
FEI Number
3043140693
Entity Name
GUANGDONG FUQIANG BEAUTY EQUIPMENT CO.,LIMITED
City/State/Country
Qingyuan Guangdong, CN
Establishment Address
Building 48, Baijia Science and Technology Innovation Park, No. 23, Chuangxing Avenue,, Henghe Street, Qingcheng District,, Qingyuan Guangdong 511500, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
guangdong fuqiang beauty equipment co.,Limited (Owner Number: 10094763)
Owner / Operator Contact Address
Building 48, Baijia Science and Technology Innovation Park, No. 23, Chuangxing Avenue,, Henghe Street, Qingcheng District,, Qingyuan, CN-GD 511500, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

G043,G045,G047,G049,G052,G053,8083,N178,A511,A515,A017,C136,C360,C454,G018,L031,L032,L033,L034,L035 Hair removal machine:FQ808,FQ808P,FQA31,FQA31-4L,FQA31-6L, FQA32, N178, G013,G035,G037, Hair growth machine:FQH01,FQH02,FQH03,FQH04,FQH05,FQH06,FQH07,FQH08,FQH09,FQH10 Pdt machine:P01,P02,P03,P04,P05,P06,P07,P08 Metal polishing machine Pico laser machine:A020,A043,A011,A32-7,C137,A509,G054,H001,PL01,PL02,PL03,PL04,PL05 Derma pen:A1-C,A1-W,A6,A6S,A7,A8S,A9,A10,A11,M5,M7,M8S,H2,H3,H6,N2-C, A6S,A7,A8S,A9,A10,A11,M5,M7,M8S,H2,H3,H6,N2-C,N2-W,V6,V7,V8,V9,V11,DRS540,X5,HN20,HN25,HR64,H24 N2-W,V6,V7,V8,V9,V11,DRS540,X5,HN20,HN25,HR64,H24 A1-C,A1-W,A6, Rf machine:FQ090,K018,M01,M02,M03,S008,S010,S014,S016 Massage machine:A009,B168,C118,152B,A057,A072,A709 Plasma pen:A019,P12,P14,P16,P18,P20,P22 Micro needle machine:A1,A2,A58,B58

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2025-12-22
OAP Laser, Comb, Hair Physical Medicine Class 2 890.5500 2025-12-22
EJQ Wheel, Polishing Agent Dental Class 1 872.6010 2025-12-22
NXF Gas, Laser Generating General, Plastic Surgery Class 1 878.4810 2025-12-22
GDF Guide, Needle, Surgical General, Plastic Surgery Class 1 878.4800 2025-12-22
PHW Cold Pack And Vibrating Massager Physical Medicine Class 1 890.5975 2025-12-22
OUH Skin Resurfacing Rf Applicator General, Plastic Surgery Class 2 878.4400 2025-12-22
HXK Holder, Needle; Orthopedic Orthopedic Class 1 888.4540 2025-12-22

Official Correspondent

dongbao chen

US Agent Details

Yuan Dan Email: service20210328@hotmail.com Phone: (805) 3513025

Related Public Records

Same Entity

guangdong fuqiang beauty equipment 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
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26
K202758 Shangdong Huamei Technology Co., Ltd. Nd: YAG Laser Therapy Systems HM-YL900 2020-11-16
K904068 Luxar Corp. LUXAR MODEL LX-20 CO2 LASER 1991-04-15
K142225 CAO Group, Inc. Pilot Elite Diode Laser 2014-09-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007 Lumenis Inc. 2
Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043140693. Last updated year: 2026. Please use registration number 3043140693 when referencing this establishment in official correspondence.
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