FDA Device Intelligence
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Basin, Emesis

FDA product code FNY · Class 1 · General Hospital

495
Registered devices
11
Adverse events
1
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-05-30DeRoyal Industries IncThe outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.

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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.