Vesalio, Inc.

Vesalio, Inc. — FDA 510(k) Submissions

Vesalio, Inc. has submitted 4 FDA 510(k) premarket notifications since 2025, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Thrombus Retriever, Catheter, Percutaneous, Neurovasculature, Aspiration Thrombectomy Catheter, Coronary Mechanical Thrombectomy With Aspiration . Use the specialty filter in the sidebar to narrow results.