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Ceribell focuses on making electroencephalography (EEG) widely accessible, more efficient, and more cost-effective. The company creates and validates an FDA cleared instant EEG system that does not require an EEG technologist or specialist interpreter, which allows for faster results and clinical decision making. The Ceribell EEG System can be set up by any healthcare provider in 6 minutes and offers a proprietary Brain Stethoscope function that dramatically simplifies interpretation of EEG results by converting brainwaves to sound so seizures can be detected by listening. Earlier diagnosis and focused treatment for patients with seizures, including non-convulsive seizures that can only be diagnosed with EEG, can significantly lower mortality, secondary brain injury, length of stay, and risk of complications.

Ceribell Company Profile

Founded in The United States around 2014, Ceribell produces noninvasive hardware and end-user software.

Ceribell makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.

BCI Categories: Open-Loop Efferent

Neurosensing Technique(s): EEG


Ceribell has 5 medical devices registered with the FDA. Here are some of them:

Examples of FDA Approved Devices ( View List)
Device ID Device Name Class Category PMA PMN
K191301 Automatic Event Detection Software For Full-Montage Electroencephalograph 2 Neurology False True
K210805 Electrode, Cutaneous 2 Neurology False True
K171459 Electrode, Cutaneous 2 Neurology False True
K170363 Reduced- Montage Standard Electroencephalograph 2 Neurology False True
K223086 Electrode, Cutaneous 2 Neurology False True



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