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Clamp, Rubber Dam

FDA product code EEF · Class 1 · Dental

882
Registered devices
301
Adverse events
1
Recalls
3
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-04-21Dentech Corp.Removing parts for safety reasons due to possible breakage.

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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.