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

FDA 510(k) Regulatory Record - VIOL Co., Ltd. General & Plastic Surgery ✕

6 devices
1-6 of 6
Cleared Aug 27, 2026
Scarlet Pro (Scarlet Pro)
K253859 · GEI
General & Plastic Surgery · 267d
Cleared Nov 26, 2024
Cellinew
K240897 · GEI
General & Plastic Surgery · 239d
Cleared Jun 23, 2022
SYLFIRM X
K213612 · GEI
General & Plastic Surgery · 220d
Cleared Apr 22, 2020
SYLFIRM X
K200185 · GEI
General & Plastic Surgery · 89d
Cleared Oct 11, 2018
SCARLET SRF
K180872 · GEI
General & Plastic Surgery · 191d
Cleared Oct 13, 2017
CELFIRM
K172023 · GEI
General & Plastic Surgery · 100d
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