Nines, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nines, Inc. has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Last cleared in 2021. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Nines, Inc. 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 - Nines, Inc.
2 devices