Enterra Medical, Inc.
Ian Scanlon is a Senior Therapy Consultant at Enterra Medical, Inc. since August 2022. Prior to this role, Scanlon served as Area Sales Manager/Director at Sonendo®, Inc. from March 2016 to August 2022, where responsibilities included leading a team of eight in driving growth for the GentleWave® root canal technology through effective coaching and sales training. From January 1999 to May 2016, Scanlon worked at Medtronic in various roles including Senior Sales Representative in Neuromodulation, and District Sales Manager, managing teams and driving sales in the medical device sector. Ian Scanlon holds a Bachelor of Arts in Psychology from Michigan State University.
Enterra Medical, Inc.
Enterra Medical is a medical device company dedicated to a singular focus: helping more people with chronic gastroparesis live better lives by advancing technology, expanding clinical science, and accelerating access to the Enterra® Therapy.* In order to increase investment and focus on the therapy, Enterra Medical was formed in 2022 and has begun the process to assume ongoing responsibility of Enterra Therapy from Medtronic. This process began with commercial responsibilities and will continue to expand to other aspects of the business. Medtronic remains a strong operational partner in this new management model and will continue to handle customer and patient support until Enterra Medical is fully equipped to assume those functions. Gastroparesis is a condition in which food moves through the stomach too slowly, causing chronic nausea and vomiting. Enterra Therapy, approved by the FDA under a Humanitarian Device Exemption in 2000, may be a surgical option for certain people who are unable to control chronic symptoms of gastroparesis.* It is the first and only implantable therapy for Gastric Electrical Stimulation, and over 15,000 people have received Enterra Therapy to help resume everyday activities. Consult with a doctor to see if Enterra Therapy may be an option for you. *Humanitarian Device. Enterra Therapy is authorized by Federal law for use in the treatment of chronic intractable (drug refractory) nausea and vomiting secondary to gastroparesis of diabetic or idiopathic etiology in patients aged 18 to 70 years. The effectiveness of this device for this use has not been demonstrated. Visit www.enterramedical.com/important-safety-information/ for important safety information.