TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO

TITANAL,STERLING SPRING,DUAL FLEX,MEMOREX,BENDALLO is an FDA 510(k)-cleared medical device (K904091) manufactured by Lancer Orthodontics, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 4, 1990. Regulation: 8.