FDA Device Intelligence
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Cabinet, Moist Steam

FDA product code IMB · Class 2 · Physical Medicine

0
Registered devices
3
Adverse events
5
Recalls
5
510(k) clearances

Recent recalls

DateFirmReason
2007-06-22Sybaritic, IncA correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D
2007-06-22Sybaritic, IncA correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D
2007-06-22Sybaritic, IncA correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D
2007-06-22Sybaritic, IncA correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on D
2007-05-15Sybaritic, IncSybaritic conducted a recall on the Hydration Station 806 because of the potential for hot water to spurt through steam ports into unit and cause burns. Also

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