Kulzer, LLC

Kulzer, LLC — FDA 510(k) Submissions

Kulzer, LLC has submitted 7 FDA 510(k) premarket notifications since 2022, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Tooth Shade, Resin, Crown And Bridge, Temporary, Resin, Cord, Retraction, Cement, Dental . Use the specialty filter in the sidebar to narrow results.