Dornier Ureteral Stent

Dornier Ureteral Stent is an FDA 510(k)-cleared medical device (K190312) manufactured by Dornier Medtech America, Inc.. 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 November 14, 2019. Regulation: 8.