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Percutaneously Delivered Prostheses And Tricuspid Valves

FDA product code NPW · Class 3 · Unknown

9
Registered devices
965
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-03-27Edwards Lifesciences, LLCLabeling update to provide warning if functionality of the valve replacement delivery system is compromised.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.