Beijing Adss Development Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Beijing Adss Development Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Fractional CO2 Laser Therapy System (FG900-S), Intensity Pulsed Light Therapy System, Diode Laser Therapy System
10
Total
10
Cleared
0
Denied
Beijing Adss Development Co., Ltd. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Beijing, CN.
Latest FDA clearance: Dec 2024. Active since 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. and Shanghai Truthful Information Technology Co., Ltd..
FDA 510(k) Regulatory Record - Beijing Adss Development Co., Ltd.
10 devices
Cleared
Dec 20, 2024
Fractional CO2 Laser Therapy System (FG900-S)
General & Plastic Surgery
192d
Cleared
Mar 15, 2024
Intensity Pulsed Light Therapy System
General & Plastic Surgery
168d
Cleared
Feb 20, 2024
Diode Laser Therapy System
General & Plastic Surgery
237d
Cleared
Jul 07, 2023
Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)
Physical Medicine
60d
Cleared
Aug 23, 2022
Picosecond Laser System (Model PS10-A and PS10-B)
General & Plastic Surgery
204d
Cleared
May 01, 2020
PDT-FACE
General & Plastic Surgery
252d
Cleared
Feb 22, 2017
ND YAG Q-switch Laser Therapy Machine
General & Plastic Surgery
224d
Cleared
Nov 16, 2016
Diode Laser Therapy Machine
General & Plastic Surgery
149d
Cleared
Oct 05, 2016
CO2 Laser Therapy Machine
General & Plastic Surgery
84d
Cleared
Aug 04, 2016
IPL Therapy Machine
General & Plastic Surgery
87d