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Dental Implant Surgical Tray

FDA product code OFY · Class 1 · Dental

212
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2010-05-18Zimmer Inc.The instructions for use contain pre-vacuum sterilization instructions that may lead to compromised sterility at the lid-kit interface location.

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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.