VertigoDx, Inc. is one of 16326 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
VertigoDx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SMARTVERTIGO™ Vestibular Assessment System
1
Total
1
Cleared
0
Denied
VertigoDx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by VertigoDx, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Imangel Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - VertigoDx, Inc.
1 devices