Our team of scientists, engineers, product managers, researchers, and designers go beyond developing products; we help clients develop multi-generational portfolios. We partner with clients to understand their market and business challenges to ensure their success.
With a focus on the innovative development of classified medical devices, we have the regulatory registrations and certifications, in-house knowledge, global suppliers and vertically integrated process in place to bring your medical device from concept to launch.
FDA Registered and ISO 13485:2016 Certified, our experience and expertise in navigating guidelines allows us to focus on human-centered design throughout the development process.