
Bisco, Inc.
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TESCERAFLO A2, MODEL T-21012P; TESCERAFLO A2 OPAQUE, MODEL T-210120P is an FDA 510(k)-cleared medical device (K030951) manufactured by Bisco, 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 June 5, 2003. Regulation: 8.