VIOL Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
VIOL Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Latest FDA clearance: Nov 2024. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by VIOL Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gms Consulting as regulatory consultant.
5 devices
Cleared
Nov 26, 2024
Cellinew
General & Plastic Surgery
239d
Cleared
Jun 23, 2022
SYLFIRM X
General & Plastic Surgery
220d
Cleared
Apr 22, 2020
SYLFIRM X
General & Plastic Surgery
89d
Cleared
Oct 11, 2018
SCARLET SRF
General & Plastic Surgery
191d
Cleared
Oct 13, 2017
CELFIRM
General & Plastic Surgery
100d