FDA product code IQO: Device, Prosthesis Alignment
IQO is the FDA product code for device, prosthesis alignment. It is a Class I device, regulated under 21 CFR 890.3025 and reviewed by the Physical Medicine panel. Devices under IQO reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 2 recalls for IQO devices.
Classification
| Field | Value |
|---|---|
| Device name | Device, Prosthesis Alignment |
| Device class | Class I |
| Regulation | 21 CFR 890.3025 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for IQO devices
2 product recalls in 2 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2012-07-27.
Frequently asked questions
What is FDA product code IQO?
IQO is the FDA product code for device, prosthesis alignment. It is a Class I device, regulated under 21 CFR 890.3025 and reviewed by the Physical Medicine panel.
What device class is IQO?
Class I, regulation 21 CFR 890.3025. Typical premarket route: 510(k) exempt.
Have IQO devices been recalled?
Yes: 2 product recalls across 2 recall events; the most recent began 2012-07-27.
Next steps
- Run an FDA pathway report with predicate devices for product code IQO
- Run a recall and safety report across every IQO manufacturer
- Watch product code IQO for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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