FDA Device Intelligence
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Drill, Dental, Intraoral

FDA product code DZA · Class 1 · Dental

10,572
Registered devices
599
Adverse events
3
Recalls
13
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-04-14Straumann USA LLCThe referred batch was produced without the laser engraving of 7 mm.
2017-07-10Zimmer Dental IncZimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard
2009-06-29Biomet 3i, LLCSome of the packages of ACT3020, drills may actually contain an ACT3220 drill.

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