Mark Schenk Vice President of Regulatory & Quality Mr. Schenk has over 20 years of experience working in the medical device industry, specifically in Quality and Regulatory Assurance roles. Mr. Schenk has been responsible for the implementation of over a dozen ISO 13485 quality systems, as well as numerous FDA and International product regulatory clearances. Previously Mr. Schenk served as Director of Quality and Regulatory Affairs for Simpact Dental. During his tenure at Simpact, he was responsible for building an ISO 13485 quality system while receiving regulatory clearances in less than a year from the company’s conception. Prior to Simpact, Mr. Schenk served in senior quality positions at several companies including Datascope Cardiac Assist Division.