Medical Device Manufacturer · US , South Bend , IN

Kulzer, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2022

Total

Cleared

Denied

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.

FDA 510(k) cleared devices by Kulzer, LLC

7 devices

1-7 of 7