
Howmedica Corp.
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MICRO-BOND HI-LIFE PROCELAIN & VIVERE is an FDA 510(k)-cleared medical device (K802235) manufactured by Howmedica Corp.. 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 25, 1980. Regulation: 8.