
Talladium, Inc.
Free shipping on orders over $99 · 30-day returns
Luminesse PMMA is an FDA 510(k)-cleared medical device (K142371) manufactured by Talladium, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 23, 2015. Regulation: 8.