Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026294985

FEI Number

3026294985

Entity Name

Weifang Dragonfly Electronic Technology Co., Ltd.

City/State/Country

Weifang Shandong, CN

Establishment Address

No. 5762 Dongfeng East Street, High-Tech Development Zone, Weifang Shandong 261061, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Weifang Dragonfly Electronic Technology Co., Ltd (Owner Number: 10086847)

Owner / Operator Contact Address

No. 5762 Dongfeng East Street, High-Tech Development Zone, Weifang, CN-SD 261061, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241547

PMA Number

N/A

All Registered Proprietary Names

DF-MASSAGE MACHINE DF-VERTICAL EMSCULPT -VE1 DF- LASER MODULE DF-CRYOLIPOLYSIS-CL1 DF-PHOTO FLASH EQUIPMENT Diode Laser Therapy Device (DF-DIODE LASER-S1)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2024-08-16
KCW	Epilator, High Frequency, Needle-Type	General, Plastic Surgery	Class 1	878.5350	2024-08-16
ILO	Pack, Hot Or Cold, Water Circulating	Physical Medicine	Class 2	890.5720	2024-08-16
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2024-08-16
GEX	Powered Laser Surgical Instrument	General, Plastic Surgery	Class 2	878.4810	2024-08-16

Official Correspondent

Ray Zhao

US Agent Details

Wen Xu Email: infor@believe-med.com Phone: (443) 8968583

Related Public Records

Same Entity

Weifang Dragonfly Electronic Technology Co., Ltd

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
K954031	R. A. Fischer Co. Corp.	COMPU-BLEND EPILATOR	1996-01-05
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

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, PASLT Fiber Delivery SystemSterileNon-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 3026294985. Last updated year: 2026. Please use registration number 3026294985 when referencing this establishment in official correspondence.