Neurent Medical is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Neurent Medical - FDA 510(k) Cleared Devices
Recent clearances: NEUROMARK System, Neuromark System
2
Total
2
Cleared
0
Denied
Neurent Medical has 2 FDA 510(k) cleared medical devices. Based in Galway, IE.
Last cleared in 2022. Active since 2021. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neurent Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurent Medical
2 devices