Telex Communications, Inc.

Telex Communications, Inc. — FDA 510(k) Submissions

Telex Communications, Inc. has submitted 50 FDA 510(k) premarket notifications since 1979, of which 50 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hearing Aid, Air-conduction, Prescription, Hearing Aid, Group And Auditory Trainer, Face Plate Hearing Aid, Masker, Tinnitus . Use the specialty filter in the sidebar to narrow results.