U-TYPE CONTRA ANGLE, U-TYPE SECTIONAL CONTRA ANGLE

U-TYPE CONTRA ANGLE, U-TYPE SECTIONAL CONTRA ANGLE is an FDA 510(k)-cleared medical device (K141125) manufactured by Handpiece Headquarters. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 22, 2014. Regulation: 8.