GUANGZHOU KONMISON TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3043153468

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
3043153468
FEI Number
3043153468
Entity Name
GUANGZHOU KONMISON TECHNOLOGY CO., LTD.
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
Room 901, AVCIT Meishi Building, No. 83 Qide Road, Jiahe Street, Baiyun District,, Guangzhou Guangdong 510440, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Guangzhou Konmison Technology Co., Ltd. (Owner Number: 10094871)
Owner / Operator Contact Address
Room 901, AVCIT Meishi Building, No. 83 Qide Road, Jiahe Street, Baiyun District,, Guangzhou, CN-GD 510440, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Diode Laser Hair Removal System Infrared blanket Plasma machine EMS massage Chair EMS Slimming Machine, Inner Ball Roller Slimming machine, Ems face lifting machine acupuncture massage pen Ultrasonic RF Iontophoresis machine EMS RF Mesotherapy device microneedling cartridges Rotation massage machine Vela Body Shape Slimming Machine, Vibration Massage Machine, Pressotherapy massage machine RF skin tightening machine, cavitation vacuum RF slimming machine, Vacuum Roller Slimming Machine micro current facial lifting machine Lipo laser slimming machine Shock wave therapy massage machine Vacuum therapy massage machine High frequency facial machine Cryo fat freezing slimming machine Plasma pen EMSlim body Sculpting Beauty Machine Multifunctional scalp care device pelvic floor therapy device Disinfecting apparatus, Sprayer, Wax heater,Tool sterilizer,Towel heater LED machines,LED facial mask, Tanning machine PDT Photon Therapy Device Blackhead removal vacuum machine, Hydra Oxygen facial machine,Micro dermabrasion machine (diamond peeling device), skin scrubber, facial brush device derma pen,derma roller,Ice roller Multifunction massager multifunctional beauty equipment Oxygen Injection Machine, Mesotherapy Device Multifunctional facial cleansing machine, multifunctional hydra dermabrasion facial skin care machine CO2 oxygen bubble machine

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2025-12-30
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2025-12-30
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2025-12-30
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use Clinical Chemistry Class 1 862.2300 2025-12-30
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2025-12-30
KNM Device, Pressure Applying Physical Medicine Class 1 890.5765 2025-12-30
PHW Cold Pack And Vibrating Massager Physical Medicine Class 1 890.5975 2025-12-30
PCM Portable Liquid Oxygen Unit Stand Physical Medicine Class 1 890.5050 2025-12-30

Official Correspondent

yingzhu shen

US Agent Details

Yuan Dan Email: service20210328@hotmail.com Phone: (805) 3513025

Related Public Records

Same Entity

Guangzhou Konmison 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
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

Similar Registrations

Registration Number Establishment Name Location
3014980477 ELEMENIC CO., LTD. Seoul, KR
3009462521 Oncore Manufacturing, LLC dba NEOTech Fremont, CA, US
3033905238 BEIJING MEGA BEAUTY TECHNOLOGY CO.,LTD. Beijing, CN
3014384451 LAMEDITECH CO., LTD. Seoul, KR
3010273372 WEIFANG KM ELECTRONICS CO., LTD Weifang Shandong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043153468. Last updated year: 2026. Please use registration number 3043153468 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.