Ids, Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ids, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PICOSECOND Nd:YAG Laser System, SHINY RPL System, SMAXEL CO2 Surgical Laser System
4
Total
4
Cleared
0
Denied
Ids, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2023. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ids, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Braunsolutions as regulatory consultant.
FDA 510(k) Regulatory Record - Ids, Ltd.
4 devices
Cleared
Dec 21, 2023
PICOSECOND Nd:YAG Laser System
General & Plastic Surgery
90d
Cleared
Oct 05, 2018
SHINY RPL System
General & Plastic Surgery
85d
Cleared
Feb 02, 2018
SMAXEL CO2 Surgical Laser System
General & Plastic Surgery
28d
Cleared
Aug 01, 2017
Q-Switched Nd:YAG Laser System
General & Plastic Surgery
112d