
Meet our Team
We are a team of innovators, scientists, and physicians, collectively driven to create therapies that change lives.
We are committed to partnering
with the SCI Community to
restore movement, function,
and independence


We benefit from a research partnership with .NeuroRestore, a collaboration between the Swiss Federal Institute of Technology (EPFL) and Lausanne University Hospital (CHUV) that develops and applies bioengineering and neurosurgical strategies to restore neurological functions, particularly those impacted by paralysis.
We also collaborate with other leading research and clinical institutions, such as those that participated in the Up-LIFT pivotal trial and other studies.
We have exclusively licensed intellectual property developed at many leading global neuroscience research institutions, such as the University of Louisville and Caltech.
Meet two of our Co-Founders
Connect with our Team
Leadership
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We are always looking for talented, mission-driven individuals in Europe and the US to help us create technologies and therapies that make a difference.
Learn about our Sustainability Initiatives
Sustainability is integral to the way we do business. The principles that guide us are highlighted in our ONWARD Medical Code and intertwined in how we operate.
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The ONWARD® Medical ARCEX® System is FDA cleared for use in the United States and CE marked in accordance with EU Medical Device Regulation 2017/745. ONWARD ARCIM® and ARCBCI™, alone or in combination with a brain-computer interface (BCI), are investigational and not available for commercial use.
Indication for Use (US): The ARCEX® System is intended to deliver programmed, transcutaneous electrical spinal cord stimulation in conjunction with functional task practice in the clinic to improve hand sensation and strength in individuals between 18 and 75 years old who present with a chronic, non-progressive neurological deficit resulting from an incomplete spinal cord injury (C2-C8 inclusive).
Indication for Use (EU): The ARCEX® System is intended to deliver programmed, transcutaneous electrical spinal cord stimulation in conjunction with functional task practice in the clinic and with take-home exercises in the home to improve hand sensation and strength in individuals between 18 and 75 years old that present with a chronic, non-progressive neurological deficit resulting from an incomplete spinal cord injury (C2-C8 inclusive).