Medicel AG

Medicel AG — FDA 510(k) Submissions

Medicel AG has submitted 6 FDA 510(k) premarket notifications since 2004, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Folders And Injectors, Intraocular Lens (iol), Lens, Guide, Intraocular . Use the specialty filter in the sidebar to narrow results.