IRIS Thermocoagulator and Digital Colposcope

IRIS Thermocoagulator and Digital Colposcope is an FDA 510(k)-cleared medical device (K202915) manufactured by Liger Medical, LLC. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 2021. Regulation: 8.