CERASORB DENTAL,CERADORB M DENTAL, CERASORB PERIO

CERASORB DENTAL,CERADORB M DENTAL, CERASORB PERIO is an FDA 510(k)-cleared medical device (K113282) manufactured by Riemser Arzeimittel AG. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 2012. Regulation: 8.