The first line is institutional rehabilitation. Atalante X and EksoNR are already used in more than 700 rehabilitation centers worldwide and hold U.S. FDA clearance and CE certification, covering stroke, spinal cord injury, multiple sclerosis and acquired brain injury. This is the most direct existing asset after the merger: within the same cohort of rehabilitation centers, the two companies were previously competing or parallel options, and now they belong to one company.
The second line is personal use. Eve provides hands-free, self-balancing mobility, while Indego Personal is a modular wearable exoskeleton; both target eligible spinal cord injury populations. This line's product form differs from institutional equipment, and the sales target shifts from rehabilitation centers to individual users, making it more dependent on payers rather than procurement budgets.
The 700-plus rehabilitation centers is an aggregate figure given by the report, and it does not distinguish how many institutions each of Atalante X and EksoNR is used in; the statistical basis and cutoff date are also unclear. The specific indication scope of the FDA clearance and CE certification is likewise only summarized by the report, with no clearance numbers or documents listed. These figures can indicate order of magnitude, but are not suitable for extrapolating the installed base of any single product.