⚠️ INVESTIGATIONAL DEVICE - Not approved for commercial distribution. Information for research and strategic partnership purposes only. Learn More →
evergait™ - Next-Generation Gait Rehabilitation
15 Years of Research • NIH Funded • 8 Publications • Patented Technology • USF Spinout

Advancing Stroke Recovery
Through Innovation

A USF Spinout Bringing Proven Rehabilitation Technology Home

First truly portable device replicating clinical-grade neuroplasticity effects for over-ground walking. Extends rehabilitation beyond clinic sessions with daily at-home practice. Developed at University of South Florida's (USF) REED Lab. Currently in regulatory pathway development.

Contact Us View Research
94% Patient Response Rate
*Investigational trials
30% Gait Speed Improvement
Clinically meaningful gains
15 Years Research Foundation
NIH/NSF funded validation
7M US Stroke Survivors
Potential to benefit from therapy

The Problem We're Solving

Stroke is the leading cause of long-term disability in the United States. Most survivors struggle with persistent gait deficits that limit independence and quality of life. Current solutions are expensive, clinic-bound, and insufficient for the daily practice needed to drive neuroplastic recovery.

Access Barrier

Clinical therapy limited to 2-3 sessions per week. Insufficient for optimal motor learning. Transportation, scheduling, and cost create additional barriers to consistent rehabilitation.

Cost Barrier

Advanced robotic systems are prohibitively expensive. Split-belt treadmills require dedicated clinic space. Only wealthy patients and large institutions can access gold-standard rehabilitation technology. Affordable home solutions are needed to democratize access.

Efficacy Gap

Home exercise programs show poor adherence. Conventional assistive devices don't provide therapeutic stimulus. No affordable solution bridges the gap between clinic-based therapy and home practice.

Our Solution

evergait™ Go is the first truly portable device that replicates clinical-grade neuroplasticity effects for over-ground walking. Passive mechanical design requires no power. Clinical-grade therapeutic benefits at a fraction of traditional clinic-based solutions.

evergait™ Go: Learn to Walk Again After Stroke

evergait Go Device - Portable Gait Rehabilitation Technology

Gait Cycle Modification

Device creates controlled displacement during gait cycle. From heel strike through swing phase, the mechanism induces therapeutic asymmetry that triggers bilateral neuroplastic adaptation.

Device Technology & Mechanics

Gait-Altering Device

Wearable shoe attachment that modifies walking patterns to trigger neuroplastic changes. Lightweight, portable design for home, clinic, or community use.

Patented Design

Patented design converts user's movement into controlled displacement. Creates therapeutic gait asymmetry triggering bilateral adaptation. No batteries required.

Smart Monitoring

IMU sensors + mobile app enable objective gait metrics and remote patient monitoring. Advanced algorithms for therapeutic feedback and outcomes tracking.

True Portability

Lightweight device fits in a bag. Use anywhere—home, clinic, or community. Only device replicating clinical-grade effects for over-ground walking.

evergait Go Device - Adjustable Components

Patented Kinetic Shape Design

Adjustable heel support and side supports with pivoting front mechanism. Four kinetic shape wheels convert user movement into controlled gait displacement. Mechanical design requires no batteries or power source.

Competitive Advantages

Truly Portable

First device for home & community use

Clinical Validation

NIH-funded with peer-reviewed publications

Protected IP

Exclusive license from USF

Market Ready

Manufacturing partners identified

Clear Pathway

Regulatory route defined

Intellectual Property

evergait™ technology is protected by patented innovations licensed from the University of South Florida. Our IP portfolio includes granted patents and additional applications covering core device functionality, manufacturing methods, and smart monitoring systems. This intellectual property represents extensive research and development at USF's REED Lab, supported by NIH and NSF funding.

Why Now?

After extensive research and clinical validation at USF, evergait™ technology is ready for commercialization. With proven clinical efficacy, strong intellectual property protection, and experienced leadership, we're positioned to transform stroke rehabilitation at scale.

Proven Technology Foundation

Extensive research foundation: Multi-million dollar federal research support (NIH/NSF)
Clinical validation: Multiple peer-reviewed publications demonstrating sustained therapeutic effects
Protected IP portfolio: Patented innovations licensed from USF
Real-world evidence: Demonstrated patient impact across multiple clinical studies
De-risked technology: Core feasibility and efficacy already established

Experienced Leadership Team

World-class inventor: Dr. Kyle Reed brings deep technical expertise and long-term commitment to product development
Proven commercial execution: Diana Shapiro's track record includes successful medical device and AI diagnostics companies
Regulatory expertise: Working with experienced FDA counsel to navigate pathway efficiently
Strategic focus: Building sustainable value through clinical evidence and market traction
Aligned incentives: Team committed to long-term success, not quick exits

Market Timing & Opportunity

Growing need: 7 million US stroke survivors with limited home therapy options
Reimbursement evolution: Increasing coverage for home-based rehabilitation technologies
Technology readiness: Manufacturing and quality systems approaching deployment stage
Strategic partnerships: Building relationships with healthcare providers and medical device leaders
Capital efficiency: Non-dilutive funding pathway supports sustainable growth

Our Approach

evergait™ combines rigorous scientific validation with experienced commercial leadership to deliver transformative rehabilitation technology. We're focused on generating clinical evidence, achieving regulatory milestones, and building strategic partnerships that create long-term value for patients, healthcare providers, and stakeholders.

Clinical Validation

Extensive research program at USF's REED Lab, supported by NIH funding. Multiple peer-reviewed publications in leading journals. Consistent efficacy demonstrated across clinical trials with stroke survivors.

Clinical Research Documentation

53-year-old stroke survivor participating in IRB-approved research study at USF REED Lab

Participant provided informed consent for research documentation. Video from IRB-approved clinical study.

Research Context: This documentation is from an investigational study. The evergait™ Go device is not cleared or approved by FDA for commercial use. Results shown are from controlled research settings and individual outcomes may vary.

Clinical Study Disclaimer

Results below are from IRB-approved investigational studies of an investigational device. Findings do not constitute FDA approval or clearance. Clinical outcomes obtained under controlled research conditions with IRB oversight and informed consent. Individual results may vary. Device safety and efficacy profile established under investigational conditions only.

2009
Concept development & initial feasibility
2012
Patent filed & kinetic shapes theory
2016
Core patent granted
2019
Clinical feasibility validated
2024
Long-term retention confirmed

Peer-Reviewed Publications

2024
One-year retention of gait speed improvement in stroke survivors after treatment with a wearable home-use gait device
Frontiers in Neurology
B. Darcy, L. Rashford, N.T. Tsai, D. Huizenga, K.B. Reed, S.J.M. Bamberg
Read Publication
2023
Gait device treatment using telehealth for individuals with stroke during the covid-19 pandemic: Nonrandomized pilot feasibility study
JMIR Formative Research
B. Darcy, L. Rashford, S.T. Shultz, N.T. Tsai, D. Huizenga, K.B. Reed, S.J. Bamberg
Read Publication
2021
Wearable gait device for stroke gait rehabilitation at home
Topics in Stroke Rehabilitation
D. Huizenga, L. Rashford, B. Darcy, E. Lundin, R. Medas, S.T. Shultz, E. DuBose, K.B. Reed
Read Publication
2020
The Relationship Between Gait Speed and Self-Reported Quality of Life in Stroke Survivors After Treatment With a Therapeutic Gait Device
Stroke
B. Darcy, L. Rashford, E. Lundin, R. Medas, T. Shultz, E. DuBose, D. Huizenga, K.B. Reed
Read Publication
2019
Relearning functional and symmetric walking after stroke using a wearable device: a feasibility study
Journal of NeuroEngineering and Rehabilitation
S. Kim, D. Huizenga, I. Handzic, R. Ditwiler, M. Lazinski, T. Ramakrishnan, A. Bozeman, D. Rose, K.B. Reed
Read Publication
2017
Device for Improving Double Limb Support, Step Length Symmetry, and Gait Speed in Hemiparetic Patients
Archives of Physical Medicine and Rehabilitation
S.H. Kim, D. Huizenga, I. Handzic, R. Edgeworth, M. Lazinski, T. Ramakrishnan, D. Rose, K.B. Reed
Read Publication
2014
Kinetic Shapes: Analysis, Verification, and Applications
ASME Journal of Mechanical Design
I. Handzic, K.B. Reed
Read Publication
2011
Design and Pilot Study of a Gait Enhancing Mobile Shoe
Journal of Behavioral Robotics
I. Handzic, E. Barno, E.V. Vasudevan, K.B. Reed
Read Publication

Complete research documentation: USF REED Lab evergait Research Page →

Regulatory & Market Readiness

Clear pathway from clinical validation to market deployment. Strategic approach balancing regulatory efficiency with sustainable reimbursement development.

Foundation Established

✓ 15 years of NIH/NSF-funded research validation - $2M+ federal investment

✓ Peer-reviewed clinical efficacy demonstrated - Published results in leading journals

✓ Patent portfolio secured with exclusive licensing - Core utility patent granted, additional IP filed

✓ ISO 13485-certified manufacturing capability identified - Scalable production partnership

✓ Quality management systems under development - FDA compliance infrastructure

Regulatory Pathway

• FDA regulatory strategy defined with experienced counsel

• Quality systems implementation in progress - Design controls and risk management

• Clinical evidence package supporting market authorization

• Preparing for regulatory submission - Documentation and testing protocols

• Post-market surveillance planning underway

Market Strategy

• Initial deployment through Florida rehabilitation networks

• Regional expansion strategy developed - Phased geographic rollout

• Reimbursement pathway analysis complete - Medicare coverage strategy

• Distribution partnerships in development - DME and specialty channels

• Real-world evidence generation planned - Supporting payor coverage

Strategic Approach

Our regulatory and commercialization strategy leverages extensive clinical validation to accelerate market entry while building sustainable reimbursement pathways. Focus on milestone achievement and evidence generation positions evergait™ for successful scaling and strategic partnerships.

Clinical Evidence Hub

Comprehensive research program with peer-reviewed publications demonstrating consistent therapeutic benefits for stroke survivors. Our evidence base continues to grow through ongoing clinical validation and real-world studies.

Published Research

8 peer-reviewed publications in leading journals demonstrating consistent clinical efficacy and sustained therapeutic effects.

View Publications

Clinical Outcomes

Proven efficacy in multiple clinical trials with sustained benefits in gait speed, symmetry, and fall reduction.

Research Documentation

Ongoing Studies

Continued clinical validation through IRB-approved research protocols expanding evidence base.

Learn More

Leadership Team

World-class research foundation meets proven commercial execution. Deep technical expertise combined with medical device go-to-market experience.

Dr. Kyle B. Reed
Kyle B. Reed, Ph.D.
Founder & Chief Technology Officer
USF Professor of Mechanical Engineering, Director of REED Lab. Inventor of evergait™ technology. Extensive patent portfolio in robotics and rehabilitation technologies, 100+ publications, extensive federal research funding (NIH/NSF). Ph.D. Northwestern University, Post-Doctoral Fellow Johns Hopkins (Haptics & Medical Robotics). Principal investigator for evergait™ research program developing and clinically testing this technology.
Diana Shapiro
Diana Shapiro
Chief Executive Officer | USF Executive in Residence
Chief Executive Officer of evergait™ LLC and USF Executive in Residence for IP Commercialization. 18+ years medical device and biotech commercialization. Former CEO Dynam.AI (Gartner Cool Vendor 2022 - AI diagnostics), Former COO PeakLogic (personalized brain treatments via TMS). Deep expertise: FDA regulatory strategy, reimbursement pathways, capital raising, M&A positioning. Leading commercialization strategy for sustainable growth.

Advisory & Support Infrastructure

Regulatory Counsel: Working with experienced FDA regulatory attorneys and reimbursement specialists for strategic guidance on market pathway and Medicare coverage development.

Manufacturing: ISO 13485-certified partner selection underway for scalable production. Quality management system implementation in progress.

R&D Collaboration: Ongoing collaboration with USF REED Lab including graduate student researchers and undergraduate engineering teams supporting technology development and clinical validation.

Sustainable Funding Approach

evergait™ is building a capital-efficient path to market through a strategic combination of non-dilutive funding and strategic partnerships. Our approach prioritizes patient access and sustainable growth while building long-term value for stakeholders.

Current Support

University Partnership: Licensed technology from University of South Florida with extensive research foundation

Seed Funding: BRAG Innovation Award recipient supporting initial development milestones

Development Funding

Federal Research Grants: Pursuing SBIR/STTR programs to support clinical validation and product development

Strategic Partnerships: Healthcare provider collaborations for pilot deployments and clinical data

Industry Collaborations: Working with medical device manufacturers and rehabilitation technology leaders

Strategic Approach

Our funding strategy emphasizes:

Non-dilutive capital first to maximize founder ownership and exit value
Clinical evidence generation to support regulatory pathway and reimbursement
Strategic partnerships that provide both capital and market access
Capital efficiency through leveraged university resources and grant funding

Why This Matters

Our capital-efficient approach allows us to focus on what matters most: delivering clinical-grade gait rehabilitation technology to patients who need it. By prioritizing non-dilutive funding and strategic partnerships, we can build sustainable value while maintaining the flexibility to pursue optimal growth pathways.

Get In Touch

Whether you're a healthcare provider interested in learning more, a researcher exploring collaboration, or a potential partner, we'd like to hear from you.

Contact Form

We typically respond within 48 business hours.

Contact Us

We welcome inquiries from healthcare providers, researchers, and potential collaborators interested in learning more about evergait™ technology.

Direct Contact

Dr. Kyle B. Reed, Ph.D.

Founder & Chief Technology Officer

Email: [email protected]
USF Email: [email protected]

Technical partnerships, research collaborations

Diana Shapiro

Chief Executive Officer | USF Executive in Residence

Email: [email protected]
USF Email: [email protected]

Business inquiries, strategic partnerships

Company Information

evergait™ LLC
Florida Registered LLC
4304 Carrollwood Village Drive
Tampa, FL 33618

Website: www.evergait.com

Regulatory Status & Important Disclaimers

Investigational Device - Critical Disclaimers

CAUTION: The evergait™ Go is an investigational medical device limited by Federal (USA) law to investigational use. It is not cleared, approved, or authorized by FDA for commercial distribution. All clinical studies conducted under IRB approval with informed consent. Information on this website is provided for research collaboration, strategic partnership, and investor due diligence purposes only. Not promotional material for medical device.

No Commercial Availability: Device not available for prescription, purchase, or clinical use outside IRB-approved research protocols. Commercial availability entirely dependent on FDA regulatory determination expected Q2 2026.