Procerus Enterprises is one of 16275 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Procerus Enterprises - FDA 510(k) Cleared Devices
Recent clearances: TruPress
1
Total
1
Cleared
0
Denied
Procerus Enterprises has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Procerus Enterprises Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ontogen Medtech as regulatory consultant.
FDA 510(k) Regulatory Record - Procerus Enterprises
1 devices