FDA Device Intelligence
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Exerciser, Non-Measuring

FDA product code ION · Class 1 · Physical Medicine

442
Registered devices
116
Adverse events
2
Recalls
43
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-03-27Amtryke LLCProduct is being recalled due to complaints of cracked frames.
2011-07-11North Coast Medical IncPotential for plastic D-ring to break during use and cause injury.

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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.