VIOL Co., Ltd. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
VIOL Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Scarlet Pro (Scarlet Pro), Cellinew, SYLFIRM X
6
Total
6
Cleared
0
Denied
VIOL Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Latest FDA clearance: Aug 2026. 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.
Regulatory submissions have been managed by Gms Consulting, GMSC Co., Ltd. and LK Consulting Group USA, Inc..
FDA 510(k) Regulatory Record - VIOL Co., Ltd.
6 devices
Cleared
Aug 27, 2026
Scarlet Pro (Scarlet Pro)
General & Plastic Surgery
267d
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