
Argen Precious Metals, Inc.
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ARGELITE 81SF+ is an FDA 510(k)-cleared medical device (K934768) 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 December 9, 1993. Regulation: 8.