
Tyrx, Inc.
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AIGIS RX N MEDIUM; AIGIS RX N LARGE is an FDA 510(k)-cleared medical device (K131007) manufactured by Tyrx, Inc.. 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 July 9, 2013. Regulation: 8.