Beijing Adss Development Co., Ltd. FDA Approvals

0 new drug approvals and 5 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2)510(k)Dec 20, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Dec 20, 2024
Intensity Pulsed Light Therapy System510(k)Mar 15, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Mar 15, 2024
Diode Laser Therapy System510(k)Feb 20, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Feb 20, 2024
Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)510(k)Jul 7, 2023Physical Medicine	Physical Medicine	510(k)Substantially Equivalent (Traditional)	Jul 7, 2023
Picosecond Laser System (Model PS10-A and PS10-B)510(k)Aug 23, 2022General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Aug 23, 2022