Aalba Dent, Inc.

Aalba Dent, Inc. — FDA 510(k) Submissions

Aalba Dent, Inc. has submitted 27 FDA 510(k) premarket notifications since 1985, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Alloy, Metal, Base, Alloy, Gold-based Noble Metal, Alloy, Other Noble Metal, Bracket, Metal, Orthodontic, Syringe, Cartridge . Use the specialty filter in the sidebar to narrow results.