DUO1 and DUO2
Jul 2024
28d
Zinnovi, Inc.
1
Total
1
Cleared
0
Denied
Zinnovi, Inc. — FDA 510(k) Submissions
Zinnovi, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, X-ray, Extraoral Source, Digital . Use the specialty filter in the sidebar to narrow results.
1 devices