
Vident
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PALLADIUS-V AND PALLADIUS-AG SEMI-PRECIOUS ALLOY is an FDA 510(k)-cleared medical device (K902863) manufactured by Vident. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 23, 1990. Regulation: 8.