Visus Health IT GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Visus Health IT GmbH - FDA 510(k) Cleared Devices
Recent clearances: JiveX (Model Number / Release: 5.4), JiveX (Model Number / Release: 5.3), JiveX
4
Total
4
Cleared
0
Denied
Visus Health IT GmbH has 4 FDA 510(k) cleared medical devices. Based in Bochum, DE.
Last cleared in 2023. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Visus Health IT GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Visus Health IT GmbH
4 devices