Gentuity, LLC

Gentuity, LLC — FDA 510(k) Submissions

Gentuity, LLC has submitted 4 FDA 510(k) premarket notifications since 2020, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Diagnostic, System, Imaging, Optical Coherence Tomography (oct) . Use the specialty filter in the sidebar to narrow results.