Atraverse Medical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Atraverse Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Cardiff By The Sea, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Atraverse Medical, Inc. 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