Venocare, Inc.

Venocare, Inc. — FDA 510(k) Submissions

Venocare, Inc. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Tubes, Vials, Systems, Serum Separators, Blood Collection . Use the specialty filter in the sidebar to narrow results.