Medical Device Manufacturer · CH , Neuchatel

Aktiia SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025

Total

Cleared

Denied

Aktiia SA has 1 FDA 510(k) cleared medical devices. Based in Neuchatel, CH.

Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Aktiia SA Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Aktiia SA

1 devices

1-1 of 1