
A.L. Miller, Inc.
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EXPAND. RETENTION ENDOSSEOUS IMPLANT is an FDA 510(k)-cleared medical device (K771858) manufactured by A.L. Miller, 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 October 19, 1977. Regulation: 8.