ARCH Medical Solutions Corp. services

When designing for Additive Manufacturing, you have to see the end result and understand how to optimize the design. Engineering and design are essential to each other and to the control and verification of product designs. With expertise on both sides of the table, Amplify has the ability to take initial concepts through full-scale product development to produce validated, high-performing solutions.

Amplify will take your idea to market, from regulatory consults to FDA 510(k) submission. By using our Quality Management System, we can repeat the desired output of excellence and compliance. Our experience includes designing, developing, and manufacturing the first six FDA 510(k) cleared orthopedic implants on the Q10 Platform.

Amplify shares your commitment to quality and regulatory compliance. We will work alongside your team to produce exceptional results through the regulatory journey. We provide superior solutions by utilizing and maintaining strong partnerships at every step of the process. Meredith May, Director of Consulting at Empirical Technologies, advises on launching safe new medical devices to market.

Working with the Best in the Business. We know exactly who to go to for testing your medical devices and product ideas. Dawn Lissy, Founder & President of Empirical Technologies and Amplify Board Member, is just one example of our industry experts we rely on to get your medical device cleared and ready for the market.