LivaNova USA, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
LivaNova USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Arvada, US.
Latest FDA clearance: Mar 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by LivaNova USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sorin Group Italia S.R.L. as regulatory consultant.
3 devices