Apryse Software Corp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apryse Software Corp - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Apryse Software Corp has 1 FDA 510(k) cleared medical devices. Based in Denver, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Apryse Software Corp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apryse Software Corp
1 devices