Medical Device Manufacturer · US , Redwood City , CA

Prenuvo - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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
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