
Ivoclar North America, Inc.
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DW207 #28G, DW207 #35F, DW207 #39LC is an FDA 510(k)-cleared medical device (K931365) 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 June 21, 1993. Regulation: 8.