Vsi Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Vsi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CLAROX plus (Model: VX-100), CLAROX
2
Total
2
Cleared
0
Denied
Vsi Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Cheongju-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vsi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lighten Bridge, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vsi Co., Ltd.
2 devices