FDA Device Intelligence
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Alloy, Amalgam

FDA product code EJJ · Class 2 · Dental

617
Registered devices
161
Adverse events
2
Recalls
74
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-12-21Ivoclar Vivadent, Inc.Affected product may not perform as expected; the amalgam powder may not triturate correctly and the physical properties (i.e. strength, compression, working ti
2014-05-29Kerr CorporationKerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directio

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