David H. Mueller is currently the Senior Principal Regulatory Affairs Specialist for Monteris Medical and has more than 30 years of medical device industry experience including Medtronic, Boston Scientific, St. Jude Medical, American Medical Systems, 3M, and private consulting.
Mr. Mueller has extensive experience in Class I, II and III cardiovascular, neurological, and urological medical devices, drug-device Combination Products, Stem-Cell devices, as well as, biocompatibility and clinical study international standards. He has published eight (8) articles in medical, and regulatory affairs, journals and has presented at 15 international and domestic medical-regulatory conferences. Mr. Mueller changed Japan’s medical device regulations, and from 2010 to 2013, was appointed to the FDA’s Neurological Devices Advisory Panel as the Industry Representative.
Mr. Mueller holds a Master of Science degree in toxicology and a Bachelor of Science degree in biology, both from the University of Minnesota.