Nuvo- Group , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Nuvo- Group , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Invu by Nuvo, INVU by Nuvo, PregSense
3
Total
3
Cleared
0
Denied
Nuvo- Group , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Last cleared in 2022. Active since 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Nuvo- Group , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Nuvo- Group , Ltd.
3 devices