Syntheon is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syntheon - FDA 510(k) Cleared Devices
Recent clearances: Syntheon LAA Exclusion System, Syntheon LAA Selection Guide
1
Total
1
Cleared
0
Denied
Syntheon has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Syntheon Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Caraballo Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Syntheon
1 devices