
Phonak, Inc.
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PHONAK LEXA 231X ITE SERIES HEARING SINSTRUMENT is an FDA 510(k)-cleared medical device (K932175) manufactured by Phonak, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 7, 1993. Regulation: 8.

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