Neuralytix, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuralytix, LLC - FDA 510(k) Cleared Devices
Recent clearances: Neuralytix iD3 System (NTX-9001)
1
Total
1
Cleared
0
Denied
Neuralytix, LLC has 1 FDA 510(k) cleared medical devices. Based in Fruita, US.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuralytix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neuralytix, LLC
1 devices