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Kaltenbach & Voigt GmbH & Co.
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INTRA LUX HEAD 3 LDSY is an FDA 510(k)-cleared medical device (K092446) manufactured by Kaltenbach & Voigt GmbH & Co.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 2, 2009. Regulation: 8.