Emily Dimambro

Emily DiMambro is a seasoned professional in regulatory affairs with extensive experience in the medical device industry, currently serving as Principal Regulatory Affairs Specialist at KORU Medical Systems since May 2022. Previous roles include Senior Regulatory Specialist and Staff Regulatory Affairs Specialist at Stryker, where contributions involved managing 510(k) submissions, maintaining compliance with EU MDR, and overseeing a major transition to a new PLM system. Emily began a regulatory career at the FDA and has also engaged in research on biocomposite materials and consulted on communication techniques. Emily holds a Bachelor of Science in Biomedical Engineering from Rensselaer Polytechnic Institute.