Visiana is one of 92 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Visiana - FDA 510(k) Cleared Devices
Recent clearances: BoneXpert
1
Total
1
Cleared
0
Denied
Visiana has 1 FDA 510(k) cleared medical devices. Based in Horsholm, DK.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Visiana Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells Cadwalader US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Visiana
1 devices