Vysioneer, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vysioneer, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VBrain, VBrain-OAR, VBrain
3
Total
3
Cleared
0
Denied
Vysioneer, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vysioneer, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vysioneer, Inc.
3 devices