ProNova Solutions is one of 16257 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
ProNova Solutions - FDA 510(k) Cleared Devices
Recent clearances: VIRTUE QA
1
Total
1
Cleared
0
Denied
ProNova Solutions has 1 FDA 510(k) cleared medical devices. Based in Maryville, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by ProNova Solutions Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - ProNova Solutions
1 devices