Tria Soft Ureteral Stent

Tria Soft Ureteral Stent is an FDA 510(k)-cleared medical device (K191609) manufactured by Boston Scientific Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 15, 2019. Regulation: 8.