Kim Rendon

Kim Rendon is a seasoned professional in regulatory affairs with extensive experience in the medical device industry. Currently serving as the Director of Regulatory Affairs at iCAD since July 2024, Kim previously held the role of Director, Regulatory Affairs at Proscia from May 2021 to September 2025. Kim's career includes significant positions at Siemens Healthineers, where responsibilities spanned from Director of Regulatory Affairs, NAM to Manager of Regulatory and Clinical Affairs, and further to Regulatory Affairs Specialist from June 2005 to May 2021. Early career experience includes roles at Triage Medical as an RA Consultant, Radiance Medical Systems as a Regulatory Affairs Specialist, Edwards Lifesciences as a Regulatory Affairs Associate, and Nobel Biocare as a Regulatory Affairs Analyst. Kim holds a B.S. in International Studies/Business from the University of Scranton, earned between 1985 and 1989.