Medical Device Manufacturer · KR , Seongnam-Si

VIOL Co., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2017

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 LK Consulting Group USA, Inc., Bt Solutions, Inc. and Gms Consulting.

FDA 510(k) Regulatory Record - VIOL Co., Ltd.

6 devices
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