Medical Device Manufacturer · US , Santa Clara , CA

Cortex, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2026

Total

Cleared

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

1-2 of 2