Inter-Med, Inc.

Inter-Med, Inc. — FDA 510(k) Submissions

Inter-Med, Inc. has submitted 7 FDA 510(k) premarket notifications since 2009, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cleanser, Root Canal, Resin, Root Canal Filling, Handpiece, Air-powered, Root Canal Irrigation, Varnish, Cavity . Use the specialty filter in the sidebar to narrow results.