FDA product code QRQ: Non-Irrigation Endosseous Dental Implant Drill Bits
QRQ is the FDA product code for non-irrigation endosseous dental implant drill bits. It is a Class I device, regulated under 21 CFR 872.3980 and reviewed by the Dental panel. Devices under QRQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
The device is intended to prepare the site for placement of endosseous dental implants. It is to be used at a low speed without irrigation.
Classification
| Field | Value |
|---|---|
| Device name | Non-Irrigation Endosseous Dental Implant Drill Bits |
| Device class | Class I |
| Regulation | 21 CFR 872.3980 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) exempt |
Recalls for QRQ devices
openFDA lists no recalls for product code QRQ.
Frequently asked questions
What is FDA product code QRQ?
QRQ is the FDA product code for non-irrigation endosseous dental implant drill bits. It is a Class I device, regulated under 21 CFR 872.3980 and reviewed by the Dental panel.
What device class is QRQ?
Class I, regulation 21 CFR 872.3980. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code QRQ
- Run a recall and safety report across every QRQ manufacturer
- Watch product code QRQ 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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