B&L L-BETA, MODEL WL-B1

B&L L-BETA, MODEL WL-B1 is an FDA 510(k)-cleared medical device (K060347) manufactured by B&L Biotech Co., Ltd.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 4, 2006. Regulation: 8.