FDA Device Intelligence
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Mirror, Mouth

FDA product code EAX · Class 1 · Dental

1,394
Registered devices
47
Adverse events
1
Recalls
12
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-03-23Sunstar Americas, Inc.Product may be contaminated with Burkholderia contaminans.

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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.