Syntheon, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syntheon, LLC - FDA 510(k) Cleared Devices
Recent clearances: LAA Exclusion System
2
Total
2
Cleared
0
Denied
Syntheon, LLC has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Last cleared in 2023. Active since 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Syntheon, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syntheon, LLC
2 devices