Avara Software is one of 12945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avara Software - FDA 510(k) Cleared Devices
Recent clearances: Avara Viewer
1
Total
1
Cleared
0
Denied
Avara Software has 1 FDA 510(k) cleared medical devices. Based in St Petersburg, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Avara Software Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Avara Software
1 devices