General Engineer (Senior Reviewer)
U.S. Food and Drug Administration
Silver Spring, Maryland, United States
Matt Beckwith is an Engineer and Senior Lead Reviewer at FDA CDRH, Office of Cardiovascular Devices. He has been with the FDA for over 5 years and specializes in the review of Class 2 and 3 interventional devices with digital health attributes including intravenous lithotripsy devices, atherectomy/ thrombectomy catheters, ablation/ denervation devices, pumps, pacemakers, and more. Matt is happy to help with any questions that relate to the regulation of software, cybersecurity, and AI/ML in medical devices. He is a Chemical Engineer by training. Prior to joining the FDA, he has worked in all areas of the medical device total product lifecycle: R&D, pre-market start up, manufacturing, post-market reliability/ quality, ect...
Disclosure(s): No financial relationships to disclose
Monday, March 9, 2026
10:24 AM - 10:32 AM EST