Titan Medical appoints Curtis R. Jensen as vice president
Mr. Jensen has more than 20 years of experience leading successful quality and regulatory affairs teams at several U.S. companies.
Prior to joining Titan, Mr. Jensen served since 2015 as senior regulatory affairs associate at EKOS where he was responsible for worldwide regulatory approval for a new CU 4.0 Control System for an ultrasound pulmonary embolism catheter.
Prior to EKOS, from 2010 to 2015 Mr. Jensen held positions of increasing responsibility at Domain Surgical including serving as Vice President of Quality and Regulatory Affairs.
At Domain Surgical he successfully submitted five 510(k) applications to the U.S. Food and Drug Administration for dissection and vessel sealing devices, and achieved CE Mark approvals.
Prior to Domain, Mr. Jensen held quality and regulatory positions at Ceramatec, GE Healthcare, Iomed, Bausch & Lomb and Bard Access Systems, among others.
Mr. Jensen holds a Master of Science degree in Applied Mathematics from Johns Hopkins University and a Bachelor of Science degree in Electrical Engineering from Utah State University. ■
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