Data / Medical devices / China / Guangdong Fuqiang Beauty Equipment Co.,limited
Guangdong Fuqiang Beauty Equipment Co.,limited: FDA-registered device maker in Qingyuan Guangdong, China, 1 510(k) clearance
Guangdong Fuqiang Beauty Equipment Co.,limited is registered with the FDA (registration 3043140693) in Qingyuan Guangdong, China. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 23, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043140693
- Address
- Building 48, Baijia Science and Technology Innovation Park, No. 23, Chuangxing Avenue, Henghe Street, Qingcheng District, Qingyuan Guangdong, China, 511500
- Owner or operator
- guangdong fuqiang beauty equipment co.,Limited (10094763)
- Roles
- Manufacturer
- First device listed
- December 22, 2025
- Registered through
- 2026
- Brand names listed
- 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, Beauty machine:FQ079,FQ094, H10,B303,A980,C014,C108,3F33,B3,K019,C169,M18,, Cavitation slimming machine:FQC01,FQC02,FQC03,FQC04,FQC05,FQC06,FQC07,FQC08,FQC09,FQC10, Cryolipolysis slimming machine:FQ032,FQ039,FQ040,P001,P002,C663,C010,C627,C667,C671, Derma pen:A1-C,A1-W,A6,A6S,A7,A8S,A9,A10,A11,M5,M7,M8S,H2,H3,H6,N2-C,, Dermatological Diode Laser Systems, Emslim machine:FQE01,FQE02,FQE03,FQE04,FQE05,FQE06,FQE07,FQE07,FQE09,FQE10, Fractional Co2 laser machine:FQZ03,C105,A021,Z03-4,Z03-5,Z03-7,A510 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cold Pack And Vibrating Massager | PHW | 1 | Manufacturer | accessdata.fda.gov |
| Gas, Laser Generating | NXF | 1 | Manufacturer | accessdata.fda.gov |
| Guide, Needle, Surgical | GDF | 1 | Manufacturer | accessdata.fda.gov |
| Holder, Needle; Orthopedic | HXK | 1 | Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Manufacturer | accessdata.fda.gov |
| Light, Surgical, Accessories | FTA | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Manufacturer | accessdata.fda.gov |
| Skin Resurfacing Rf Applicator | OUH | 2 | Manufacturer | accessdata.fda.gov |
| Ultrasound, Skin Permeation | NRJ | 2 | Manufacturer | accessdata.fda.gov |
| Wheel, Polishing Agent | EJQ | 1 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 23, 2021 | K202257 | Dermatological Diode Laser Systems | GEX | Substantially Equivalent | Zhuolu Jontelaser Manufacturing Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light, Surgical, Accessories
- All makers of Laser, Comb, Hair
- All makers of Skin Resurfacing Rf Applicator
- All makers of Cold Pack And Vibrating Massager
- All makers of Powered Laser Surgical Instrument
Updated April 23, 2021. 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.