Cerrozone, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cerrozone, LLC - FDA 510(k) Cleared Devices
Recent clearances: CerroZone Mini
1
Total
1
Cleared
0
Denied
Cerrozone, LLC has 1 FDA 510(k) cleared medical devices. Based in Maryland Heights, US.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cerrozone, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cerrozone, LLC
1 devices