Beijing Adss Development Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241670Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2)December 20, 2024
K233307Intensity Pulsed Light Therapy SystemMarch 15, 2024
K231896Diode Laser Therapy SystemFebruary 20, 2024
K231318Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)July 7, 2023
K220268Picosecond Laser System (Model PS10-A and PS10-B)August 23, 2022
K192295PDT-FACEMay 1, 2020
K161926ND YAG Q-switch Laser Therapy MachineFebruary 22, 2017
K161692Diode Laser Therapy MachineNovember 16, 2016
K161925CO2 Laser Therapy MachineOctober 5, 2016
K161286IPL Therapy MachineAugust 4, 2016