Ilooda Co,., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ilooda Co,., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Secret MAX Multi-platform RF System, SUPER VELOCE, Secret Pro
16
Total
16
Cleared
0
Denied
Ilooda Co,., Ltd. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Gwonseon-Gu, Suwon-Si, KR.
Latest FDA clearance: Nov 2024. Active since 2015.
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 Bt Solutions, Inc., Mtechgroup and Kathy Maynor Consulting.
FDA 510(k) Regulatory Record - Ilooda Co,., Ltd.
16 devices
Cleared
Nov 21, 2024
Secret MAX Multi-platform RF System
General & Plastic Surgery
209d
Cleared
Aug 13, 2024
SUPER VELOCE
General & Plastic Surgery
61d
Cleared
Dec 14, 2023
Secret Pro
General & Plastic Surgery
73d
Cleared
Sep 15, 2023
PENTO Nd:YAG and Alexandrite laser system
General & Plastic Surgery
87d
Cleared
Sep 27, 2022
MTX-C1
General & Plastic Surgery
410d
Cleared
Sep 23, 2022
reepot Nd
General & Plastic Surgery
31d
Cleared
Jun 24, 2022
Secret Duo
General & Plastic Surgery
267d
Cleared
Jun 09, 2022
ACUTRON
General & Plastic Surgery
433d
Cleared
Apr 23, 2021
Secret Duo
General & Plastic Surgery
274d
Cleared
Sep 06, 2019
Secret RF Smartcure Applicator with electrodes
General & Plastic Surgery
372d
Cleared
Jul 27, 2018
RetiCapture
Ophthalmic
260d
Cleared
Dec 01, 2017
CuRAS Nd:YAG Laser
General & Plastic Surgery
64d
Cleared
Aug 09, 2017
Fraxis
General & Plastic Surgery
29d
Cleared
Jun 13, 2017
SECRET RF
General & Plastic Surgery
131d
Cleared
Oct 28, 2016
FRAXIS DUO
General & Plastic Surgery
266d
Cleared
Aug 06, 2015
VIKINI Diode Laser System
General & Plastic Surgery
90d