Inamed Development Co.

Inamed Development Co. — FDA 510(k) Submissions

Inamed Development Co. has submitted 7 FDA 510(k) premarket notifications since 1989, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Suction, Single Patient Use, Portable, Nonpowered, Surgeon's Gloves, Dilator, Rectal, Expander, Surgical, Skin Graft, Apparatus, Suction, Operating-room, Wall Vacuum Powered . Use the specialty filter in the sidebar to narrow results.