Miltex, Inc.

Miltex, Inc. — FDA 510(k) Submissions

Miltex, Inc. has submitted 23 FDA 510(k) premarket notifications since 1982, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, File, Pulp Canal, Endodontic, Instrument, Filling, Plastic, Dental, Clip, Implantable, Probe, Periodontic . Use the specialty filter in the sidebar to narrow results.