Nexstim Oyj is one of 27 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Nexstim Oyj - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nexstim Oyj has 2 FDA 510(k) cleared medical devices. Based in Helsinki, FI.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nexstim Oyj Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nexstim Oyj
2 devices