Mend Technologies, Inc.

Mend Technologies, Inc. — FDA 510(k) Submissions

Mend Technologies, Inc. has submitted 3 FDA 510(k) premarket notifications since 1988, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tampon, Menstrual, Unscented, Table And Attachments, Operating-room, Table, Surgical With Orthopedic Accessories, Ac-powered . Use the specialty filter in the sidebar to narrow results.