Tom Sundlof leverages more than two decades of government experience, including key leadership roles at the Food and Drug Administration (“FDA”), as well as legal roles at the U.S. House of Representatives, to provide clients with counsel on regulatory, compliance, and enforcement matters for medical devices, combination products, and other FDA-regulated industries. Tom previously served as Associate Chief Counsel and Assistant Deputy Chief Counsel (Acting) in the FDA’s Office of the Chief Counsel, where he advised on high-profile regulatory actions, enforcement, and policy development.
