
Austenal, Inc.
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MYERSON'S PERMASOFT SOFT RELINE MATERIAL is an FDA 510(k)-cleared medical device (K933468) manufactured by Austenal, 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 January 4, 1994. Regulation: 8.