
Johnson & Johnson Professionals, Inc.
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ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM is an FDA 510(k)-cleared medical device (K871295) manufactured by Johnson & Johnson Professionals, 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 May 28, 1987. Regulation: 8.