INNOVATE.

VALIDATE.

SOLVE.

FDA Breakthrough Device Designation.
Patented nVRT Technology.

INNOVATE.

VALIDATE.

SOLVE.

FDA Breakthrough Device Designation.
Patented nVRT Technology.

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Groundbreaking Technology

Our patented technology utilizes non-invasive Vestibular Resonance Therapy (nVRT) to impact the vestibular system.

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First Vertigo Wearable

We are developing a noninvasive and easy-to-use wearable solution for chronic vertigo, which is suffered by over 11 million Americans.

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Non-Invasive, Non-Pharmacological

The compact, headworn wearable device requires no surgery, advanced patient calibration, or complex fittings.

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Designed To Be Safe

Through development and clinical studies, our device has been used on over 600 subjects, with zero reportable serious device-related adverse events.

Clinical Studies

Recruitment for our at-home vertigo study has closed, but we have current and upcoming studies that may interest you.

Click “Interested? Click here!” to complete the 3-question survey to receive updates when enrollment opportunities open. Learn more here.

Working With

Working
With

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Latest News

Otolith Labs Rounds Out Executive Team with Hiring of Chief Clinical Officer

Otolith Labs Rounds Out Executive Team with Hiring of Chief Clinical Officer

Kevin Franck, PhD, MBA appointed as Otolith Labs’ Chief Clinical Officer.

Otolith Expands Leadership Team with CCO and New Board Member

Otolith Expands Leadership Team with CCO and New Board Member

Otolith appointed Dan Wagner as Chief Commercial Officer and Raphael Michel to Otolith’s Board of Directors.

Mark Cuban-Backed Otolith Labs Just Raised Another $20M

Mark Cuban-Backed Otolith Labs Just Raised Another $20M

Technical.ly interviews Otolith’s CEO Sam Owen about the pressing need for a new treatment option for chronic vertigo.

Otolith Receives FDA Breakthrough Device Designation

Otolith Receives FDA Breakthrough Device Designation

Otolith Labs announces closing of $3.3 Million in seed funding, as well as receiving “Breakthrough Device” Designation from FDA.

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