Morpheus AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Morpheus AG - FDA 510(k) Cleared Devices
Recent clearances: Rebellion, Phantom Multi-Bite Kerrison Rongeur, Rebellion, Rebellion, Phantom Multi-Bite Kerrison Rongeur
3
Total
3
Cleared
0
Denied
Morpheus AG has 3 FDA 510(k) cleared medical devices. Based in Spaichingen, DE.
Last cleared in 2023. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Morpheus AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Morpheus AG
3 devices