Gi Bionics, LLC

Gi Bionics, LLC — FDA 510(k) Submissions

Gi Bionics, LLC has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Esophageal Motility, Anorectal Motility, And Tube . Use the specialty filter in the sidebar to narrow results.