Bend IT Technologies, Ltd.

Bend IT Technologies, Ltd. — FDA 510(k) Submissions

Bend IT Technologies, Ltd. has submitted 4 FDA 510(k) premarket notifications since 2019, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Percutaneous, Neurovasculature, Catheter, Intravascular, Diagnostic, Catheter, Continuous Flush . Use the specialty filter in the sidebar to narrow results.