Ceribell

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

FDA

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

Hardware

• BrainScope

Links

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