HAIDARI BEAUTY TECHNOLOGY (BEIJING) CO., LTD

FDA Device Registration & Listing · Beijing, CN · Registration 3023850562

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3023850562
FEI Number
3023850562
Entity Name
HAIDARI BEAUTY TECHNOLOGY (BEIJING) CO., LTD
City/State/Country
Beijing, CN
Establishment Address
Room 110, Building 1, No.18, Jingxing Street, Nanshao Town, Changping District, Beijing 102299, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Haidari Beauty Technology (Beijing) Co., Ltd (Owner Number: 10095703)
Owner / Operator Contact Address
Room 110, Building 1, No.18, Jingxing Street, Nanshao Town, Changping District, Beijing, CN-BJ 102299, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Facial Hydrogen Oxygen Bubble System CO2 Laser Treatment Machine (CFR3M1) CFR2M1, CFR3H1, CFR3M2, CFR3H2, CFR2H1, CFR2H2, CFR1M1, CFR1M2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2026-04-16
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2026-04-16

Official Correspondent

Yuehong Zhong

US Agent Details

Xu Wen Email: infor@believe-med.com Phone: (443) 4438968

Related Public Records

Same Entity

Haidari Beauty Technology (Beijing) 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
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
K142225 CAO Group, Inc. Pilot Elite Diode Laser 2014-09-12

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, PA***SLT Fiber Delivery System***Sterile***Non-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 3023850562. Last updated year: 2026. Please use registration number 3023850562 when referencing this establishment in official correspondence.
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