FDA product code NFP: Device, Dental Sonography, For Diagnosis Of Tmj / Mpd Disorders
NFP is the FDA product code for device, dental sonography, for diagnosis of tmj / mpd disorders. It is a Class II device, regulated under 21 CFR 872.2050 and reviewed by the Dental panel. Devices under NFP reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Device, Dental Sonography, For Diagnosis Of Tmj / Mpd Disorders |
| Device class | Class II |
| Regulation | 21 CFR 872.2050 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) |
Recalls for NFP devices
openFDA lists no recalls for product code NFP.
Frequently asked questions
What is FDA product code NFP?
NFP is the FDA product code for device, dental sonography, for diagnosis of tmj / mpd disorders. It is a Class II device, regulated under 21 CFR 872.2050 and reviewed by the Dental panel.
What device class is NFP?
Class II, regulation 21 CFR 872.2050. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NFP
- Run a recall and safety report across every NFP manufacturer
- Watch product code NFP 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.
All Dental product codes · FDA product code lookup · 510(k) database search · 510(k) review times