Envision Endoscopy

Envision Endoscopy — FDA 510(k) Submissions

Envision Endoscopy has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Grasping/cutting Instrument, Non-powered, Endoscopic Tissue Approximation Device . Use the specialty filter in the sidebar to narrow results.