Kulzer, LLC - FDA 510(k) Cleared Devices

Kulzer, LLC has 7 FDA 510(k) cleared medical devices. Based in South Bend, US.

Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Kulzer, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.