Atraverse Medical - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Atraverse Medical has 2 FDA 510(k) cleared medical devices. Based in Cardiff By The Sea, US.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Atraverse Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
2 devices