Neoventa Medical AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Neoventa Medical AB - FDA 510(k) Cleared Devices
Recent clearances: Goldtrace Fetal Spiral Electrode (FSE) (CNS000004)
1
Total
1
Cleared
0
Denied
Neoventa Medical AB has 1 FDA 510(k) cleared medical devices. Based in M?lndal, SE.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Neoventa Medical AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neoventa Medical AB
1 devices