STARTUP PROFILE

Neurovalens

COUNTRY
UK
FOUNDED
2013
CATEGORY
Neuromodulation
Developing FDA-cleared, non-invasive vestibular neurostimulation wearables (Modius Sleep, Modius Stress) to treat insomnia, anxiety, and metabolic disorders.
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Neurofounders Insights
$   Funding   -
Seed
MODALITY
Nerve stimulator
FORM FACTOR
Headset/cap
INTERFACE DEPTH
Non-invasive
INDICATION
Sleep
TARGET USER
Patients
REGULATORY STAGE
FDA cleared (510k)
Neurovalens is positioned around non-invasive vestibular neurostimulation, an unusual modality that gives it a distinct identity across sleep, anxiety, and metabolic applications. Its FDA-cleared products provide tangible commercial validation, even if the mechanism remains less familiar than mainstream nerve stimulation.
Mentioned in Market Notes
MOST RECENT COVERAGE
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1
Tracking Neurotech Startups
1 May – 26 May 2026

The FDA granted de novo classification to Neurovalens' Modius Spero just two days ago, making it the world's first neuromodulation device authorized to treat symptoms associated with PTSD. The device delivers electrical vestibular system stimulation behind each ear for 30 minutes daily, targeting deep brain regions associated with stress response. Neurovalens now holds FDA authorizations across four indications: insomnia, anxiety, weight management, and PTSD. See the Double Click section below for a closer look.

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Neurovalens