Cortex, Inc.

Cortex, Inc. — FDA 510(k) Submissions

Cortex, Inc. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intracardiac Mapping, High-density Array . Use the specialty filter in the sidebar to narrow results.