Aktiia SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Aktiia SA - FDA 510(k) Cleared Devices
Recent clearances: G0 Blood Pressure Monitoring System (G0)
1
Total
1
Cleared
0
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Aktiia SA
1 devices