Aesculap Instruments Corp.

Aesculap Instruments Corp. — FDA 510(k) Submissions

Aesculap Instruments Corp. has submitted 13 FDA 510(k) premarket notifications since 1977, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drill, Dental, Intraoral, Sterilizer, Steam, Bur, Dental, Bone Mill, Apparatus, Suction, Operating-room, Wall Vacuum Powered . Use the specialty filter in the sidebar to narrow results.