
Ivoclar North America, Inc.
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R&D PROJECT DW269#25 is an FDA 510(k)-cleared medical device (K001469) manufactured by Ivoclar North America, 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 July 4, 2000. Regulation: 8.