Prenuvo is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prenuvo - FDA 510(k) Cleared Devices
Recent clearances: Prenuvo Body Composition
1
Total
1
Cleared
0
Denied
Prenuvo has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Prenuvo Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Innolitics as regulatory consultant.
FDA 510(k) Regulatory Record - Prenuvo
1 devices