
Astron Dental Corp.
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2ND MODIFIED VINYLAC PRESS PACK DENTURE RESIN is an FDA 510(k)-cleared medical device (K874025) manufactured by Astron Dental Corp.. 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 22, 1987. Regulation: 8.