Vivosonic, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Vivosonic, Inc. has 5 FDA 510(k) cleared medical devices. Based in Stamford, US.
Latest FDA clearance: Dec 2024. Active since 2001. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Vivosonic, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Vivosonic, Inc.
5 devices
Cleared
Dec 19, 2024
Integrity V500 (Integrity, Integrity with VEMP)
Ear, Nose, Throat
85d
Cleared
Apr 04, 2008
VIVOSONIC NEUROSCREEN
Neurology
86d
Cleared
Jan 24, 2005
INTEGRITY, MODEL V500
Neurology
45d
Cleared
Oct 27, 2003
VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER
Ear, Nose, Throat
27d
Cleared
Jul 18, 2001
VIVO 200 DPS VIVOSCAN
Ear, Nose, Throat
264d