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Finger Cot

FDA product code LZB · Class 1 · General Hospital

79
Registered devices
1
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-03-31American Surgical CompanyProduct packaging defective compromising sterility

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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.