STARTUP PROFILE

Aurenar

COUNTRY
United States
FOUNDED
2024
CATEGORY
Neuromodulation
Developing a non-invasive, single-use transauricular vagus nerve stimulation device to reduce inflammation-driven complications in ICU stroke patients.
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Neurofounders Insights
$   Funding   -
Seed
MODALITY
VNS
FORM FACTOR
Wearable (body)
INTERFACE DEPTH
Non-invasive
INDICATION
Stroke
TARGET USER
Patients
REGULATORY STAGE
Investigational
Transauricular vagus nerve stimulation gives Aurenar a low-friction entry point into acute ICU care, targeting inflammation-driven secondary brain injury rather than building a broad neuromodulation platform from day one. FDA Breakthrough Device status and pilot data from Washington University carry it further along the translation path than most seed-stage neuromodulation companies typically reach this early.
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MOST RECENT COVERAGE
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6
BCI Goes Commercial
21 July – 4 August 2026

Aurenar closed an oversubscribed $5.7M seed round co-led by the American Heart Association's Go Red for Women Venture Fund and Solas BioVentures. The St. Louis company's V-Link platform delivers non-invasive vagus nerve stimulation through the outer ear to reduce cerebral vasospasm, a dangerous narrowing of blood vessels that follows a brain haemorrhage. A university trial reported a more than 40% reduction in moderate-to-severe vasospasm. The round follows the device's June FDA Breakthrough Device designation and funds development toward a pivotal trial.

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