Cortex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cortex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OptiMap Catheter - 60mm (OPTI-CATH2-60), OptiMap Catheter - 50mm (OPTI-CATH2-50)
2
Total
2
Cleared
0
Denied
Cortex, Inc. has 2 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cortex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cortex, Inc.
2 devices