If you are a rehabilitation device manufacturer struggling to offer patients real independence — this project developed an exoskeleton with 13 degrees of freedom (versus an industry average of 4) controlled entirely by the user's own upper body movements. That means no crutches, no attendant, and simpler electronics that bring production costs down. It opens a product line for outpatient and home-use markets that current exoskeletons cannot reach.
Hands-Free Exoskeleton Giving Paraplegic Users Full Independent Walking Control
Imagine a wearable robotic suit that lets someone with paralyzed legs walk again — but instead of a computer deciding every step, the person controls their legs by moving their arms naturally. Most exoskeletons on the market need crutches or a helper standing by, and they only bend at a few joints. This one has 13 moving joints (competitors average just 4), so movements look and feel far more natural. Because the control system is simpler — your arms tell your legs what to do — the whole device is cheaper, lighter, and less likely to malfunction.
What needed solving
Millions of people with paraplegia depend on wheelchairs because current exoskeletons are expensive, require crutches or an attendant, and move stiffly with very few joint movements. This keeps patients dependent and limits rehabilitation options. The market needs a genuinely autonomous, affordable exoskeleton that users can operate independently in daily life.
What was built
Tecnimusa developed a lower-limb exoskeleton with 13 degrees of freedom that is controlled by the user's upper body movements, eliminating the need for crutches or external supervision. The only documented deliverable is the public project website providing information on objectives, approach, and results.
Who needs this
Who can put this to work
If you are a rehabilitation clinic investing in walking therapy for spinal cord injury patients — this exoskeleton eliminates the need for a trained operator to supervise every session. With movement driven by the patient's upper limbs rather than pre-programmed trajectories, therapy sessions become more intuitive and require fewer staff. The 13 degrees of freedom enable more natural gait patterns, potentially improving patient outcomes.
If you are an insurer covering long-term disability or workplace injury rehabilitation — this device could reduce the duration and cost of inpatient rehabilitation by enabling earlier independent mobility. Its simpler control system makes it fail-safer than competitors with maximum 10 degrees of freedom, reducing liability risk. Faster return-to-function means lower ongoing claim costs for mobility-impaired policyholders.
Quick answers
What does this exoskeleton cost compared to existing ones?
The project objective states that simpler computing requirements result in a cheaper device, easing access to the general public. No specific price point is provided in the available data, but the reduced electronics complexity is a concrete cost driver. Based on available project data, the commercial price would need to be confirmed directly with Tecnimusa.
Can this be manufactured at industrial scale?
Tecnimusa is an engineering SME founded in 2011 in Murcia, Spain, specializing in combining different technologies into custom solutions. The project was funded under SME Instrument Phase 2, which targets close-to-market innovation. Scaling production would likely require manufacturing partnerships or licensing, as the consortium is a single SME.
What is the IP situation and can we license this technology?
As a single-partner SME Instrument project, all intellectual property would be held by Tecnimusa S.L. Based on available project data, licensing arrangements or distribution partnerships would need to be negotiated directly with them. The unique upper-limb control mechanism is the core differentiator worth exploring.
Has this been tested with real patients?
The project objective describes the intent to develop all necessary stages to introduce the exoskeleton to market. However, the available deliverable data only lists a public project website. Based on available project data, clinical testing details would need to be confirmed with the coordinator.
What regulatory approvals does it have?
No regulatory approval information is available in the project data. Medical exoskeletons require CE marking in Europe and FDA clearance in the US. The SME Instrument Phase 2 funding typically supports activities toward market introduction, which would include regulatory steps.
How does this integrate with existing rehabilitation programs?
The exoskeleton's upper-limb control system means patients do not need crutches or a supervising operator, which simplifies integration into clinical workflows. With 13 degrees of freedom versus an average of 4 in competitors, it supports more natural movement patterns. Based on available data, specific clinical protocol integration details are not documented.
Who built it
This is a single-company project: Tecnimusa S.L., a Spanish engineering SME founded in 2011 in Murcia, funded through the SME Instrument Phase 2. With 1 partner from 1 country and 100% industry composition, all development knowledge and IP sit within one organization. There are no university or research institute partners, which means the technology was developed entirely in-house. For a potential business partner, this simplifies negotiations — there is one decision-maker — but also means due diligence should verify whether Tecnimusa has the clinical validation and manufacturing capacity to deliver at scale, or whether they are seeking partners for exactly those capabilities.
- TECNIMUSA S.L.Coordinator · ES
Tecnimusa S.L. is an engineering SME based in Murcia, Spain. Contact can be established through their company website or the CORDIS project page.
Talk to the team behind this work.
Want an introduction to the HUMEXE team? SciTransfer can arrange a direct meeting with Tecnimusa to discuss licensing, distribution, or integration partnerships.