Rxsight, Inc.

Rxsight, Inc. — FDA 510(k) Submissions

Rxsight, Inc. has submitted 5 FDA 510(k) premarket notifications since 2018, of which 5 received clearance as substantially equivalent to a predicate device.

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