Tria Firm Ureteral Stent

Tria Firm Ureteral Stent is an FDA 510(k)-cleared medical device (K163399) 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 June 21, 2017. Regulation: 8.