Data / Medical devices / China / Weifang Dragonfly Electronic Technology Co., Ltd.
Weifang Dragonfly Electronic Technology Co., Ltd.: FDA-registered device maker in Weifang Shandong, China, 1 510(k) clearance
Weifang Dragonfly Electronic Technology Co., Ltd. is registered with the FDA (registration 3026294985) in Weifang Shandong, China. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 13, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026294985
- Address
- No. 5762 Dongfeng East Street, High-Tech Development Zone, Weifang Shandong, China, 261061
- Owner or operator
- Weifang Dragonfly Electronic Technology Co., Ltd (10086847)
- Roles
- Manufacturer
- First device listed
- August 16, 2024
- Registered through
- 2026
- Brand names listed
- DF- LASER MODULE, DF-1927nm Laser, DF-755NM ALEXANDRITE LASER, DF-AESTHETIC COSMETIC BEAUTY MACHINE, DF-CO2 FRACTIONAL LASER -CF1, DF-CRYOLIPOLYSIS-CL1, DF-Fiber Coupled Laser, DF-Fractional RF and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Arthrogram Tray | OII | 2 | Manufacturer | accessdata.fda.gov |
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Epilator, High Frequency, Needle-Type | KCW | 1 | Manufacturer | accessdata.fda.gov |
| Gas, Laser Generating | NXF | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Marker, Skin | FZZ | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Water Circulating | ILO | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | 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 |
|---|---|---|---|---|---|---|
| August 13, 2024 | K241547 | Diode Laser Therapy Device (DF-DIODE LASER-S1) | GEX | Substantially Equivalent | Weifang Dragonfly Electronics Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Marker, Skin
- All makers of Powered Laser Surgical Instrument
- All makers of Epilator, High Frequency, Needle-Type
- All makers of Brush, Dermabrasion, Powered
Updated August 13, 2024. 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.