Weifang Dragonfly Electronic Technology Co., Ltd.
Registered establishment in Weifang, Shandong, China. 9 device types.
Weifang Dragonfly Electronic Technology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Marker, Skin, Arthrogram Tray and 7 other device types. Its earliest product listing with the FDA dates from 2024.
Registration
| Status | Registered |
|---|---|
| Registration expires | 2026 |
| Registration number | 3026294985 |
| FEI number | 3026294985 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 潍坊蜻蜓电子科技有限公司 |
|---|---|
| Source | customs registration record |
Location
| City | Weifang |
|---|---|
| Province | Shandong |
| Address | No. 5762 Dongfeng East Street, High-Tech Development Zone |
| Postal code | 261061 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Arthrogram Tray | Class 2 | DF-Hifu | 2026 | 1 |
| Brush, Dermabrasion, Powered | Class 1 | DF-IPL, DF-Hydra Facial | 2024 | 65 |
| Epilator, High Frequency, Needle-Type | Class 1 | DF- Laser Module | 2024 | 4 |
| Gas, Laser Generating | Class 1 | DF-Fiber Coupled Laser, DF-1927nm Laser, DF-Nd:yag Laser, DF-755NM Alexandrite Laser, DF-CO2 Fractional Laser -CF1, DF-Picosecond Pulsed Laser -P1 | 2024 | 17 |
| Lamp, Infrared, Therapeutic Heating | Class 2 | DF-Fractional RF, DF-Photo Flash Equipment | 2024 | 235 |
| Marker, Skin | Class 1 | DF-Aesthetic Cosmetic Beauty Machine | 2024 | 55 |
| Massager, Therapeutic, Electric | Class 1 | DF-Vertical Emsculpt -VE1, DF-Massage Machine | 2024 | 437 |
| Pack, Hot Or Cold, Water Circulating | Class 2 | DF-CRYOLIPOLYSIS-CL1 | 2024 | 45 |
| Powered Laser Surgical Instrument | Class 2 | Diode Laser Therapy Device (DF-DIODE LASER-S1) | 2024 | 92 |
Clearances
No clearance names Weifang Dragonfly Electronic Technology Co., Ltd. as applicant. One is held by another company and named on this establishment’s own product listings: the device is cleared under that company’s 510(k) and listed under this registration.
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K241547 | 2024-08-13 | GEX | Traditional | Weifang Dragonfly Electronics Technology Co., Ltd. |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.