Tonya Wilbon

Tonya A. Wilbon is the Assistant Director for the Postmarket Industry and Consumer Education Teams, Division of Industry and Consumer Education (DICE), Office of Communication, Information Disclosure, Training and Education (OCITE), Center for Devices and Radiological Health (CDRH). Tonya leads DICE’s efforts to educate and inform the medical device and radiological health industry on its FDA regulatory requirements for marketing medical devices and radiation-emitting products. In addition, she leads the division’s efforts to educate and inform consumers, health care professionals, and patients on issues with these medical devices and radiation-emitting products. Ms. Wilbon has been with FDA for over 25 years with more than 10 years of clinical laboratory experience. She initially began with the FDA as a Microbiology Scientific Reviewer for CDRH's Office of In Vitro Diagnostics and Radiological Health (OIR) and served as the Quality System Specialist within OIR. Ms. Wilbon also currently serves as an FDA instructor for the Association for the Advancement of Medical Instrumentation (AAMI) and serves on FDA’s Content Advisory Group as an instructor for FDA Investigators and Staff. Ms. Wilbon received a Bachelor of Science Degree in Microbiology from Howard University and is a certified Microbiologist by the American Society of Clinical Pathology (ASCP).