Kaltenbach & Voigt GmbH

Kaltenbach & Voigt GmbH — FDA 510(k) Submissions

Kaltenbach & Voigt GmbH has submitted 9 FDA 510(k) premarket notifications since 2011, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Controller, Foot, Handpiece And Cord, Caries Detector, Laser Light, Transmission, Handpiece, Air-powered, Dental, Handpiece, Belt And/or Gear Driven, Dental, Unit, Operative Dental . Use the specialty filter in the sidebar to narrow results.