RiverLon (Nylon) Suture

RiverLon (Nylon) Suture is an FDA 510(k)-cleared medical device (K152795) manufactured by Riverpoint Medical. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 2015. Regulation: 8.