Robotic Gait Training That Fits Your Budget and Your Ward
Clinical-grade lower-limb exoskeleton systems at 40-60% below Western brand pricing. A complete rehabilitation pathway -- from intensive early gait retraining through to corridor walking support and ankle/foot drop management.
- Gait trainer, hip assist, and ankle/AFO -- one supplier, one documentation package
- Accessed through your local distributor, or contact GaitExo directly to find one
- Pilot program available: validate clinical fit before committing to full purchase
What Robotic Gait Training Delivers for Your Patients and Your Team
The figures below are based on clinical feedback from rehabilitation settings in China where these devices are in active use. They are provided for illustration purposes only. Individual patient outcomes depend on diagnosis, severity, clinical protocol, therapist practice, and patient-specific factors. GaitExo makes no claims about outcomes in specific clinical environments outside China. Please assess clinical suitability with your own clinical team.
| Metric | Manual Therapy | With Gait Exoskeleton |
|---|---|---|
| Gait training duration per session | 15-20 minutes | 40+ minutes (assisted) |
| Therapist physical effort | High -- manual support required | Reduced -- device provides support |
| Training consistency | Variable per session | Standardised, repeatable parameters |
| Patients per therapist per day | 4-6 patients | Potentially 8-10 patients |
Therapists reported more consistent gait cycles per session compared to manual support alone. Repetition quality improved with device guidance.
Longer training durations reported without increased therapist physical fatigue. Patients completed more assisted steps per session.
Extended corridor walking distances reported with hip assist support during transition-phase rehabilitation.
All data points above are based on clinical team feedback from Chinese rehabilitation settings. They are not controlled clinical studies and have not been peer-reviewed. Individual results vary significantly depending on patient profile, clinical setting, and therapy protocol.
One Portfolio for the Full Lower-Limb Rehab Journey
Three complementary device categories covering the full rehabilitation pathway -- from early intensive gait retraining through transition-phase walking support to ankle and foot drop management. You do not need to purchase all three at once.
Intensive Early Gait Retraining
For stroke and SCI patients requiring comprehensive lower-limb gait support during the intensive rehabilitation phase.
- Weight range: 50-100kg · Height range: 155-185cm (model dependent)
- Multiple training modes: overground, treadmill, and balance training
- Real-time gait data and clinician dashboard
- Body weight support system integrated
Corridor and Community Walking Support
For patients moving from intensive gait training toward functional corridor walking and semi-independent ambulation.
- Lightweight soft exosuit design -- under 3-minute donning
- Powered hip flexion assistance for natural gait pattern
- Suitable for ward corridors, outpatient settings, and day rehabilitation
- Complements gait trainer use -- not a replacement
Foot Drop and Ankle Control Management
For patients with foot drop, ankle weakness, or impaired dorsiflexion -- during clinical gait training and in preparation for discharge and daily walking.
- Powered and passive modes available
- Gait-phase adaptive control for natural dorsiflexion timing
- Suitable for both clinical training sessions and longer daily wear
- Completes the lower-limb rehabilitation pathway
You do not need to purchase all three at once. Many hospital partners start with the gait trainer, then add hip assist and ankle solutions as budget and clinical experience develop. We help design a phased acquisition plan that matches your ward structure and patient volume.
24-36 Month Payback -- A Conservative Estimate
The calculator below uses conservative illustrative assumptions. Actual payback depends on your therapy billing rates, patient volume, session frequency, reimbursement environment, and local operational costs. Use this as a starting framework for internal discussion -- not as a financial guarantee or projection.
Your Department Parameters
Estimated Results
Calculated using default inputs above. German DRG reimbursement for neurorehabilitation is complex and variable -- consult your finance team for market-specific billing figures. Therapy billing rates vary significantly across European markets.
From First Contact to Patients on Device
Device Arrival & First Patients
- 1 device delivered, full technical documentation provided
- Remote staff training session completed (2-3 hours)
- First 5-10 patients selected with your clinical team
- Baseline data collection begins
Timeline: weeks 1-4 from delivery
Clinical Integration & Data Review
- Therapist feedback collected and workflow adjusted
- Patient session data reviewed against baseline
- Technical issues identified and resolved with GaitExo support
- IT and billing integration confirmed if applicable
Timeline: month 2-3
Expand Across Your Department
- Decision on additional units based on pilot data
- Expand to second device category (hip assist or ankle/AFO)
- Broader department integration planning begins
- Reference site documentation initiated for procurement records
Timeline: month 4 onwards
How We Reduce Your Risk at Every Stage
No Upfront Certification Burden
Our products are exported as rehabilitation training equipment under HS 8479.89. You are not required to initiate medical device registration before running a pilot. Your regulatory advisor determines what is required in your country and clinical context.
- Products classified as rehabilitation training equipment for import
- Full technical documentation provided for your regulatory assessment
- ISO 13485 manufacturing quality certificates available on request
- GaitExo provides intended use statements and device specifications to support your advisor's review
GaitExo is not the local medical device registrant. Classification and registration decisions are made by you and your regulatory advisors in accordance with national regulations.
Pilot Commitment Structure
What a pilot commitment actually looks like -- in writing, before any order is placed.
- Start with 1 device at pilot pricing -- no commitment to further units
- 30-day technical support included post-delivery at no additional cost
- Option to return device for full credit if it fails to meet agreed written technical specifications
- Scale to additional units only after your clinical team confirms satisfaction
- All pilot terms confirmed in the purchase agreement before shipment
Return eligibility applies to technical specification failures only, not clinical outcome expectations. Full terms discussed and confirmed in writing prior to order placement.
Questions from Clinical and Procurement Teams
The questions we hear most often from rehabilitation department heads, equipment managers, and procurement officers -- before a first pilot discussion.
What types of patients are suitable for gait exoskeleton training?
Gait exoskeletons are used in rehabilitation settings for patients with neurological and orthopaedic conditions affecting walking ability. Common patient groups include stroke survivors with hemiparesis, individuals with incomplete spinal cord injuries, patients recovering from lower-limb orthopaedic surgery, people with multiple sclerosis or Parkinson's disease, and geriatric patients with general mobility decline. Patient selection depends on cognitive status, body dimensions, residual motor function, and rehabilitation goals. These are clinical tools for supervised therapy sessions -- patient suitability should be assessed by your clinical team using your own clinical protocols.
Do your products have CE marking as medical devices?
No. Our products are not currently CE marked as medical devices under EU Medical Device Regulation (MDR 2017/745). They are exported as rehabilitation training equipment under HS Code 8479.89. Whether local medical device registration is required in your country depends on your national regulations and how you intend to classify and use the devices clinically. This determination must be made by your regulatory affairs advisor. We provide complete technical documentation -- including ISO 13485 quality certificates, technical specifications, and intended use statements -- to support that assessment.
What documentation do you provide for our procurement committee?
We provide a comprehensive documentation package that covers the requirements of most European hospital procurement processes. This includes: commercial invoice and packing list, certificate of origin, ISO 13485 quality management certificate from the manufacturing partner, full technical specifications, English-language instructions for use (IFU), intended use statement, and a compliance summary document. We also provide a downloadable Compliance and Trade Summary PDF specifically designed to support internal procurement committee reviews. Additional documentation -- such as risk management summaries or specific test reports -- is available on request.
Can we access GaitExo systems directly, or only through a distributor?
In most cases, hospitals access GaitExo systems through a local medical device distributor in their country -- the distributor handles local sales, after-sales support, and any local compliance processes. If you do not currently have a distributor relationship, contact us directly and we will identify whether we have a partner in your market or help facilitate an introduction. In some cases, we can discuss direct supply arrangements depending on your location and order volume.
How long does it take from order to device delivery?
Standard lead time from confirmed purchase order is 4-8 weeks, depending on product model and configuration. Sea freight from China to major European ports (Hamburg, Rotterdam, Gothenburg, Copenhagen) takes approximately 25-35 days. Your local distributor coordinates delivery to your facility from the port. Air freight is available for urgent requirements at additional cost. For pilot units, we work with distributors to expedite delivery where possible.
What training and ongoing support is provided after delivery?
We provide English-language technical documentation and instructions for use with every device. After delivery, a remote training session (typically 2-3 hours via video call) is available for your clinical team and equipment staff. Ongoing technical Q&A support is available through your distributor and, for more complex technical questions, directly with GaitExo. We can also support your team with remote training for new staff as your programme grows. On-site training can be arranged through your distributor depending on your location.
Have a clinical or procurement question not answered here? Contact us directly →
Tell Us About Your Rehabilitation Ward
Share a few details about your facility -- bed count, patient mix, current equipment, and budget range. We will propose a realistic starting configuration and connect you with a local distributor if needed.
Clinical data and performance figures referenced on this page are based on feedback from rehabilitation settings in China where GaitExo's manufacturing partners' devices are in active clinical use. They are illustrative only and do not constitute controlled clinical research, peer-reviewed studies, or outcome guarantees. GaitExo's products are not CE marked as medical devices under EU MDR 2017/745. Local medical device classification and registration requirements vary by country and intended use -- all such determinations must be made by the importer and their regulatory advisors. GaitExo acts as a trading and branding partner only.