Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017200975

FEI Number

3017200975

Entity Name

BEIJING SUPERLASER TECHNOLOGY CO., LTD.

City/State/Country

Beijing, CN

Establishment Address

1st Floor, Building 3, No.2 Zhongfu Street, Economic and Technological Industrial Zone, Xihongmen Town, Daxing District, Beijing 100076, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Beijing Superlaser Technology Co., Ltd. (Owner Number: 10075781)

Owner / Operator Contact Address

1st Floor, Building 3, No.2 Zhongfu Street, Economic and Technological Industrial Zone, Xihongmen Town, Daxing District, Beijing, CN-BJ 100076, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K192516

PMA Number

N/A

All Registered Proprietary Names

Multi-modality workstation AAD Dual Light Multi-modality workstation AAD Dual Light(SL-HV92) ND:YAG Laser SL-NY602 ND:YAG Laser SL-NY603 ND:YAG Laser SL-NY755 Diode laser therapy device VADER-SL Diode laser therapy device VADER Diode Laser 808nm SL-HR10

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ONF	Powered Light Based Non-Laser Surgical Instrument With Thermal Effect	General, Plastic Surgery	Class 2	878.4810	2020-06-27
GEX	Powered Laser Surgical Instrument	General, Plastic Surgery	Class 2	878.4810	2020-06-27
GEX	Powered Laser Surgical Instrument	General, Plastic Surgery	Class 2	878.4810	2025-09-07
GEX	Powered Laser Surgical Instrument	General, Plastic Surgery	Class 2	878.4810	2020-06-26

Official Correspondent

Shuang Shi

US Agent Details

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

Related Public Records

Same Entity

Beijing Superlaser 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
K192521	Shangdong Huamei Technology Co., Ltd.	Intense Pulsed Light Treatment System	2019-12-06
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

Similar Registrations

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3043047259	BLINK BRIGHT MEDICAL, INC.	Houston, TX, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017200975. Last updated year: 2026. Please use registration number 3017200975 when referencing this establishment in official correspondence.