CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO

CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO is an FDA 510(k)-cleared medical device (K051443) manufactured by Curasan Ag, Frankfurt Facility. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 21, 2005. Regulation: 8.