FDA Device Intelligence
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Dress, Surgical

FDA product code FYE · Class 1 · General, Plastic Surgery

23
Registered devices
12
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-05-08DePuy Orthopaedics, Inc.LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove packages were mispackaged, with right handed, large sized glove p

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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.