
Mentor Corp.
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SILICONE DOUBLE COIL URETERAL STENT WITH SUTURE is an FDA 510(k)-cleared medical device (K862539) manufactured by Mentor Corp.. 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 September 8, 1986. Regulation: 8.