Aaron Lynch

Aaron Lynch, MS, currently serves as a Regulatory Affairs Specialist III at Boston Scientific, where responsibilities include supporting the DeVoro Medical, Inc. acquisition and authoring FDA 510(k) submissions for clot management technologies. Prior experience includes a role as Senior Regulatory Affairs Specialist at Vyaire Medical, where Lynch authored a 510(k) submission for the AirLife DuoTherm Humidification System, and various regulatory affairs positions at Smith+Nephew. Early career highlights include developing FDA Best Practices Guides as a Policy and Investment Analyst Intern at AdvaMed and collaborating on assistive device designs during academic projects. Lynch holds a Master of Science in Engineering Management from Tufts University and two Master's and a Bachelor's degree in Biomedical Engineering from The George Washington University.