
Argen Precious Metals, Inc.
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ARGENCO 16 TYPE I DENTAL GOLD ALLOY is an FDA 510(k)-cleared medical device (K902901) manufactured by Argen Precious Metals, 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 August 8, 1990. Regulation: 8.