
Mentor Corp.
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MENTOR DBL-COIL INDWELLING POLYURETHANE URETERAL- is an FDA 510(k)-cleared medical device (K850176) 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 February 27, 1985. Regulation: 8.