Viasonix , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Viasonix , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Yonkers, US.
Latest FDA clearance: Dec 2024. Active since 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Viasonix , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Viasonix , Ltd.
6 devices
Cleared
Dec 18, 2024
Falcon/Xpress (Falcon/Xpress)
Cardiovascular
105d
Cleared
Jan 25, 2021
Dolphin/IQ, Dolphin/4D and Dolphin/MAX with Dolphin/XF robot accessory
Radiology
129d
Cleared
Dec 19, 2019
LiteWalk
Physical Medicine
90d
Cleared
May 16, 2019
Dolphin/IQ, Dolphin/4D and Dolphin/MAX
Radiology
29d
Cleared
Nov 14, 2017
Dolphin/IQ and Dolphin/4D
Radiology
237d
Cleared
Jul 15, 2011
FALCON
Radiology
56d