Aesyra SA is one of 141 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Aesyra SA has 1 FDA 510(k) cleared medical devices. Based in Lausanne, CH.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Aesyra SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aesyra SA
1 devices