Kettenbach GmbH & Co. KG has 14 FDA 510(k) cleared dental devices. Based in Eschenburg, DE.

Latest FDA clearance: Sep 2026. Active since 2008.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Kettenbach GmbH & Co. KG

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