BEIJING BEAUTEMAX TECHNOLOGY LIMITED

FDA Device Registration & Listing · Beijing, CN · Registration 3043657394

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
3043657394
FEI Number
3043657394
Entity Name
BEIJING BEAUTEMAX TECHNOLOGY LIMITED
City/State/Country
Beijing, CN
Establishment Address
Room 102, No. 89, Yangpo Village, Baoshan Town, Huairou District, Beijing 101400, CN
Establishment Type(s)
Foreign Private Label Distributor,Manufacture Medical Device
Owner / Operator
Beijing Beautemax Technology Limited (Owner Number: 10095045)
Owner / Operator Contact Address
Room 102, No. 89, Yangpo Village, Baoshan Town, Huairou District, Beijing, CN-BJ 101400, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Elight System; IPL; SHR Aqua Facial Hydrogen Oxygen Bubble System ELECTRONIC MUSCLE STIMULATOR Microneedle Fractional RF System laser, cellulite appearance - Cryolipolysis Beauty ND:yag Q-Switch Laser System; Picosecond System Skin Analyzer System Long Pulse Alexandrite Laser System CO2 Fractional Laser System Radio frequency and vacuum machine IPL DPL SHR Elight Therapy Machine HIFEM Beauty System High Intensity Focus Ultrasound (HIFU) System

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 2026-01-19
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2026-01-19
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2026-01-19
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2026-01-19
OYW Laser, Cellulite Appearance General, Plastic Surgery Class 2 878.4810 2026-01-19
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2026-01-19
HCJ Device, Skin Potential Measurement Neurology Class 2 882.1560 2026-01-19
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2026-01-19
NXF Gas, Laser Generating General, Plastic Surgery Class 1 878.4810 2026-01-19
PBX Massager, Vacuum, Radio Frequency Induced Heat General, Plastic Surgery Class 2 878.4400 2026-01-19
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2026-01-19
OUP Powered Surgical Instrument For Improvement In The Appearance Of Cellulite General, Plastic Surgery Class 2 878.4790 2026-01-19
PZC Ablation System, High Intensity Focus Ultrasound (Hifu), Soft Tissue Unknown Class N N/A 2026-01-19

Official Correspondent

Jingya Zhang

US Agent Details

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

Related Public Records

Same Entity

Beijing Beautemax Technology Limited
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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04

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 3043657394. Last updated year: 2026. Please use registration number 3043657394 when referencing this establishment in official correspondence.
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