Apoller Flow Light Cure Flowable Composite

Apoller Flow Light Cure Flowable Composite is an FDA 510(k)-cleared medical device (K180463) manufactured by Greenway Yw, LLC. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 13, 2018. Regulation: 8.