Neuvotion Receives FDA Clearance for NeuStim™ Providing Non-Invasive, High-Resolution Stimulation for the Hand After Stroke or Spinal Cord Injury

STAMFORD, Conn., Feb. 11, 2025 /PRNewswire/ -- Neuvotion, Inc. is an early-stage medical device company developing AI-driven neuromodulation technologies and products for use in the neurorehabilitation, brain-computer interface (BCI), and physical therapy markets. Neuvotion has received FDA 510(k) clearance for their first product, NeuStim™, a non-invasive, surgery-free wearable that electrically stimulates muscles dynamically and with high-precision.

“At Neuvotion we are developing highly innovative technologies built on two decades of scientific research yielding effective and easy-to-use products,” said Chad Bouton, Neuvotion’s founder and CEO. “We are extremely excited about NeuStim™, our first product, which we believe will be a game-changer in the neuromodulation, brain-computer interface, and neurorehabilitation markets.”

“We have been very impressed with Professor Bouton’s groundbreaking foundational research and Neuvotion’s highly innovative approach,” said Michael Spigel, PT, MHA, President & CEO of Good Shepherd Rehabilitation. “We look forward to continuing as a clinical research partner with Neuvotion. We feel that NeuStim™ is truly revolutionary and will help produce improved outcomes in stroke and spinal cord injury rehabilitation.”

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