Engage engineers, clinicians, and regulatory experts who’ve built and launched devices in the real world, so you can get there faster and with more confidence.
Brains Behind Breakthrough Devices
Medical device innovation demands expertise shaped in the field. MDisrupt connects you with proven engineers, clinicians, regulatory strategists, and go-to-market leaders who’ve launched successful devices in real-world settings.
Experts Who’ve Built Devices That Clinicians Trust
Work with strategists and commercial leaders with 10+ years in med device, experienced in regulatory submissions, CE Mark approvals, and driving adoption.
Built-In Flexibility for Medtech Teams
Whether you need early feedback on design inputs or end-to-end guidance, MDisrupt adapts to your pace. Use Health Expert Hourly for targeted insight, Health Expert OnDemand to embed fractional talent, or Health Expert Hire to build device teams.
Real-world perspective and hands-on experience across clinical workflows, adoption, and safety, ensuring your device fits into care delivery.
Confidently navigate 510(k), De Novo, and CE Mark pathways with experts who know how to translate innovation into compliance.
Guide and implement product strategy from design controls through V&V and launch—ensuring cross-functional readiness and regulatory alignment.
Design and execute studies built for both regulatory review and commercial success, supporting claims, market differentiation, and faster approvals.
Experts in coding, coverage, and value strategy who’ve secured payer alignment for medical devices across U.S. and global markets.
Shape strategies for hospital and health system adoption—from evaluation and budgeting to enterprise-wide implementation.
"MDisrupt is not an outsourced company to Xandar Kardian. They are part of our team. Healthtech startups are extremely challenging. Having a trusted partner like MDisrupt to help us along the journey enables our company to focus on what we do bet and push forward successfully."
MDisrupt delivers the insight and execution to bring market-ready devices into clinical use and secure regulatory approval.
