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Syringe, Cartridge

FDA product code EJI · Class 2 · Dental

341
Registered devices
34
Adverse events
1
Recalls
45
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-02-11Milestone Scientific, Inc.Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.

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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.