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Ceribell

Point of care electroencephalography systems for rapid seizure detection.

What they do

The company manufactures a simplified headband and diagnostic platform that enables rapid bedside detection of non-convulsive status epilepticus. Emergency departments and intensive care units purchase this system to make fast, informed decisions regarding brain monitoring. On September 30, 2026 Ceribell announced FDA 510(k) clearance for new software adding Alpha-Delta Ratio and Relative Alpha trending, burst suppression monitoring and amplitude-integrated EEG, with no age restriction; the features are expected via software update in the first half of 2027. On November 2, 2026 Ceribell announced commercial launch of its Delirium Monitoring Solution following FDA 510(k) clearance on December 9, 2025. It supports clinician delirium screening and monitoring on the seizure-monitoring platform and headband. Ceribell trades on Nasdaq as CBLL. CMS NTAP is up to $2,171 per eligible Medicare case from October 1, 2026, not a guaranteed payment for every case.

Source announcement

People in this update

  • Jane ChaoCo-founder and CEOSource
  • Juliana Barr, MDProfessor emerita, Stanford University School of Medicine; quoted in the launch releaseSource

The record

Vertical
Medical Devices
Sub-segment
Point of care diagnostics
Product type
Device
Stage
Public
Headquarters
Sunnyvale, USA
Region
North America
Founded
2014
Total funding
$110M raised

Notable investors: The Rise Fund, Tee Grove Ventures, Redmile Group.

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