
Rexton, Inc.
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LONG LIFE RX-12 is an FDA 510(k)-cleared medical device (K960295) manufactured by Rexton, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 21, 1996. Regulation: 8.

Ansell
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McKesson
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Hollister
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