FDA product code QQF: Skin Microneedling Manual/Automated Device (Export Only)
QQF is the FDA product code for skin microneedling manual/automated device (export only). It is a Not classified device, reviewed by the General and Plastic Surgery panel. Devices under QQF reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
For one-time (1X) use by qualified clinical professionals to cause bio-active effect(s) in skin for aesthetic improvement.
Classification
| Field | Value |
|---|---|
| Device name | Skin Microneedling Manual/Automated Device (Export Only) |
| Device class | Not classified |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for QQF devices
openFDA lists no recalls for product code QQF.
Frequently asked questions
What is FDA product code QQF?
QQF is the FDA product code for skin microneedling manual/automated device (export only). It is a Not classified device, reviewed by the General and Plastic Surgery panel.
What device class is QQF?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code QQF
- Run a recall and safety report across every QQF manufacturer
- Watch product code QQF 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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