Michael Ryan

Michael Ryan

Regulatory Advisor, FDA

Mike Ryan is a Regulatory Advisor at the FDA’s Center for Devices and Radiological Health (CDRH) in the Office of Device Evaluation (ODE) with 12 years of regulatory experience. Mike leads various regulatory projects on premarket review policy, including the 510(k) device modifications policy, and advises FDA staff and industry on CDRH’s premarket program. Prior to his role as a Regulatory Advisor, Mike served as a lead reviewer and biomedical engineer in ODE for six years.