Zenflow Spring Scope
Sep 2025
162d
Zenflow, Inc.
1
Total
1
Cleared
0
Denied
Zenflow, Inc. — FDA 510(k) Submissions
Zenflow, Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cystoscope And Accessories, Flexible/rigid . Use the specialty filter in the sidebar to narrow results.
1 devices