Data / Medical devices / China / Guangzhou Konmison Technology Co., Ltd.
Guangzhou Konmison Technology Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 2 510(k) clearances
Guangzhou Konmison Technology Co., Ltd. is registered with the FDA (registration 3043153468) in Guangzhou Guangdong, China. It lists 10 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 25, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043153468
- Address
- Room 901, AVCIT Meishi Building, No. 83 Qide Road, Jiahe Street, Baiyun District, Guangzhou Guangdong, China, 510440
- Owner or operator
- Guangzhou Konmison Technology Co., Ltd. (10094871)
- Roles
- Manufacturer
- First device listed
- December 30, 2025
- Registered through
- 2026
- Brand names listed
- 2940nm Erbium laser device 1550nm & 1927nm Dual Fractional Laser device NIR milk light skin Rejuvenation Machine, Blackhead removal vacuum machine, Hydra Oxygen facial machine,Micro dermabrasion machine (diamond peeling device),, CO2 oxygen bubble machine, Diode Laser Hair Removal System, Disinfecting apparatus, Sprayer,, ELECTRONIC MUSCLE STIMULATOR, EMSlim body Sculpting Beauty Machine Multifunctional scalp care device pelvic floor therapy device, Hair scalp detector machine PRP machine Laser hair growth machine Thulium laser machine and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Cold Pack And Vibrating Massager | PHW | 1 | Manufacturer | accessdata.fda.gov |
| Colorimeter, Photometer, Spectrophotometer For Clinical Use | JJQ | 1 | Manufacturer | accessdata.fda.gov |
| Device, Pressure Applying | KNM | 1 | Manufacturer | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Manufacturer | accessdata.fda.gov |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Portable Liquid Oxygen Unit Stand | PCM | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 25, 2024 | K241860 | Diode Laser Hair Removal System | GEX | Substantially Equivalent | Beijing Winkonlaser Technology Limited | accessdata.fda.gov |
| July 13, 1998 | K980040 | ELECTRONIC MUSCLE STIMULATOR - MICROSTIM J-1304D | IPF | Substantially Equivalent | Nisha Communication Industries | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Muscle, Powered
- All makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- All makers of Portable Liquid Oxygen Unit Stand
- All makers of Massager, Therapeutic, Electric
- All makers of Powered Laser Surgical Instrument
- All makers of Disinfectant, Medical Devices
Updated September 25, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.