FDA Device Intelligence
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Needle, Acupuncture, Single Use

FDA product code MQX · Class 2 · General Hospital

4,338
Registered devices
13
Adverse events
1
Recalls
91
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2007-11-28Marknew ProductsMarketed without 510(k)

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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.