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BrightWater Medical’s ConvertX Biliary Stent System receives FDA clearance

Press releases may be edited for formatting or style | March 25, 2019 Cardiology

The ConvertX Biliary Stent System is part of BrightWater Medical’s ConvertX Stent Family, which includes the company’s innovative ConvertX Nephroureteral Stent System cleared by the FDA for treatment of ureteral obstructions. That system enables the IR to eliminate a second invasive interventional procedure in treating patients with severe ureteral blockages.

The ConvertX Stent Family was featured at the Advanced Interventional Management (AIM) Symposium in New York City in November 2018 as the lead presentation during the “New and Innovative Technologies” section. BrightWater received its medical device manufacturing license from the California Department of Public Health and manufactures the ConvertX Stent Family at its facility in Temecula, CA.

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About BrightWater™ Medical
BrightWater Medical is a mid-stage medical device company uniquely positioned to significantly impact treatments provided by interventional radiologists. The company was founded by Dr. Bob Smouse, Professor of Radiology & Surgery, University of Illinois College of Medicine. Dr. Smouse is a leading interventional radiologist, clinician, academic and entrepreneur, with more than 20 years of experience in interventional radiology, endovascular surgery and clinical research. The company is developing additional ConvertX-based products for other staged procedure treatments in interventional radiology.

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