Zinnovi, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zinnovi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DUO1 and DUO2
1
Total
1
Cleared
0
Denied
Zinnovi, Inc. has 1 FDA 510(k) cleared medical devices. Based in Schaumburg, US.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Zinnovi, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Global Quality and Regulatory Services as regulatory consultant.
FDA 510(k) Regulatory Record - Zinnovi, Inc.
1 devices