Ceribell

U.S. Food and Drug Administration building
BrainSpace gets 510(k) nod for brain fluid management system and more FDA clearances
By Jessica Hagen | 12:54 pm | January 07, 2026
Ceribell received breakthrough device designation for its LVO stroke detection monitor, and Naox Technologies secured 510(k) clearance for its in-ear EEG device.
Person at a desk looking at a computer
Seer Medical receives FDA 510(k) for its at-home epilepsy diagnosis aide
By Jessica Hagen | 04:48 pm | September 26, 2022
The company’s Seer Home device allows for potential epilepsy diagnosis through at-home data collection.
Healthcare professionals examining computer screen.
Ceribell raises $50M for seizure monitoring and detection technology
By Jessica Hagen | 01:50 pm | September 22, 2022
The company will use the funding to support the commercial expansion of its product.