Kettenbach GmbH & Co. KG is one of 470 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Kettenbach GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Profisil Free, Visalys® Bulk Fill 1 x 4 g Syringe (15060), Profisil Fluoride Varnish Combi pack (14801), Profisil Fluoride Varnish Normal pack mint (14802), Profisil Fluoride Varnish Normal pack berry (14804), Profisil Fluoride Varnish Normal pack unflavored (14806), Profisil Fluoride Varnish Sample pack (14800)
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.