
Neotract, Inc.
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UroLift System (UL400 and UL500) is an FDA 510(k)-cleared medical device (K173087) manufactured by Neotract, 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 December 27, 2017. Regulation: 8.