Vuno, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Vuno, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage, VUNO Med-DeepBrain
2
Total
2
Cleared
0
Denied
Vuno, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Nov 2024. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vuno, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vuno, Inc.
2 devices