Ocuject, LLC

Ocuject, LLC — FDA 510(k) Submissions

Ocuject, LLC has submitted 8 FDA 510(k) premarket notifications since 2017, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Syringe, Piston, Low Dead Space Needle, Single Lumen, Hypodermic, Ophthalmic Syringe . Use the specialty filter in the sidebar to narrow results.