Our process - How we work
We believe in rigorous medical device development and cutting-edge biomedical engineering to deliver life-changing solutions. Our process combines clinical expertise with advanced technology to create innovative rehabilitation and assistive devices that truly improve patients' lives.

Research & Analysis
We begin every medical device project with comprehensive clinical research and patient needs analysis, working closely with healthcare professionals to understand the real-world challenges and requirements.
Our interdisciplinary team of biomedical engineers, clinicians, and researchers conduct extensive literature reviews, analyze existing solutions, and identify gaps in current rehabilitation technology. We study neural pathways, muscle activation patterns, and biomechanical principles to ensure our solutions are grounded in solid scientific foundation.
Through patient interviews, clinical observations, and regulatory analysis, we develop a comprehensive requirements specification that guides the entire development process while ensuring compliance with medical device standards.
Included in this phase
- Clinical needs assessment
- Regulatory compliance review
- Biomechanical analysis
- Patient journey mapping
- Technology feasibility studies
- Safety risk assessment

Design & Development
Based on our research findings, we develop comprehensive engineering specifications and begin the iterative design process. Our approach combines cutting-edge signal processing with intuitive human-machine interfaces to create truly revolutionary medical devices.
Each project follows rigorous design controls with dedicated project managers ensuring clear communication and milestone tracking. Our embedded systems engineers work alongside biomechanical specialists to develop real-time control algorithms that achieve sub-200ms response times while maintaining safety and reliability.
We maintain continuous collaboration with clinical partners throughout development, conducting regular design reviews and incorporating feedback to ensure the final product meets both technical specifications and real-world usability requirements.
Myotron's engineering expertise and attention to medical device standards gave us confidence that our innovative exoskeleton would meet both clinical needs and regulatory requirements.

Validation & Deployment
The final phase involves comprehensive clinical validation and regulatory submission. We work with certified testing facilities to ensure all safety and efficacy requirements are met before deployment.
Our validation process includes extensive user testing with real patients in controlled clinical environments. We measure key performance indicators such as adaptation time, control accuracy, and patient satisfaction to validate the device's effectiveness.
We provide comprehensive training programs for healthcare professionals and establish robust support systems to ensure successful integration into clinical practice and optimal patient outcomes.
Included in this phase
- Clinical Trials. Comprehensive testing with target patient populations to validate safety, efficacy, and usability under real-world conditions.
- Regulatory Submission. Complete documentation and submission packages for medical device approval in target markets including CE marking and FDA clearance.
- Training & Support. Comprehensive training programs for healthcare providers and ongoing technical support to ensure optimal patient outcomes.
Our values - Advancing healthcare through innovation
We are committed to developing medical devices that genuinely improve patients' lives. Our core values guide every decision we make, from initial research through clinical deployment, ensuring we deliver solutions that are safe, effective, and transformative.
- Clinical Excellence. Every project begins with deep clinical understanding and is validated through rigorous testing with real patients and healthcare professionals.
- Regulatory Compliance. We maintain the highest standards of medical device development, ensuring all products meet or exceed regulatory requirements for safety and efficacy.
- Patient-Centered. Our design process prioritizes patient needs, comfort, and outcomes, creating intuitive solutions that enhance quality of life and independence.
- Scientific Rigor. All our innovations are grounded in peer-reviewed research and validated through comprehensive testing and clinical evidence.
- Collaborative. We foster partnerships with leading medical institutions, clinicians, and researchers to ensure our solutions address real-world healthcare challenges.
- Transformative Impact. We focus on breakthrough technologies that create paradigm shifts in rehabilitation and assistive care, delivering measurable improvements in patient outcomes.
Ready to transform rehabilitation technology?
Our offices
- Istanbul
Maslak Mahallesi, Büyükdere Cad.
No:255 Nurol Plaza, 34398 Şişli, Istanbul - Ankara
ODTÜ Teknokent, Silikon Blok
06800 Çankaya, Ankara - Bursa
Uludağ Üniversitesi Teknokent
16059 Nilüfer, Bursa