Gi Supply, Inc.

Gi Supply, Inc. — FDA 510(k) Submissions

Gi Supply, Inc. has submitted 2 FDA 510(k) premarket notifications since 2020, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Submucosal Injection Agent, Pump, Portable, Aspiration (manual Or Powered) . Use the specialty filter in the sidebar to narrow results.