JoAnn Kuhne

Vice President Regulatory Affairs and Quality Assurance

JoAnn Kuhne joined Sientra in 2006. Ms. Kuhne has more than twenty years of global regulatory and clinical experience. Prior to joining Sientra, Ms. Kuhne served as Senior Director, Regulatory Affairs at Inamed Corporation (now Allergan Medical) where she was instrumental in the company’s efforts to obtain PMA approval for the company’s silicone gel breast implants. Before Inamed, Ms. Kuhne was Director of Regulatory & Clinical Affairs at Medtronic PS Medical, leading the company’s global regulatory and clinical efforts for its neurosurgical implants. Preceding her career at Medtronic PS Medical and Inamed, Ms. Kuhne spent several years in the orthopedic implant industry as Manager of Regulatory Affairs for Smith and Nephew Orthopedics and Intermedics Orthopedics. Ms. Kuhne received her BSN from Northern Michigan University in Marquette, Michigan and an MSN from the University of North Carolina at Chapel Hill. She is a member of the Sigma Theta Tau International Honor Society and is board certified in Regulatory Affairs. Ms. Kuhne is an active volunteer at the Santa Ynez Valley Therapeutic Riding Center and is a sponsor for Threshold Ministries and Impact 2818.