
Auric Hearing Systems, Inc.
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RETROX is an FDA 510(k)-cleared medical device (DEN020003) manufactured by Auric Hearing Systems, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 19, 2002. Regulation: 8.

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