FDA product code NFR: Device, Jaw Tracking, For Diagnosis Of Tmj / Mpd Disorders
NFR is the FDA product code for device, jaw tracking, for diagnosis of tmj / mpd disorders. It is a Class II device, regulated under 21 CFR 872.2060 and reviewed by the Dental panel. Devices under NFR reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Device, Jaw Tracking, For Diagnosis Of Tmj / Mpd Disorders |
| Device class | Class II |
| Regulation | 21 CFR 872.2060 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) |
Recalls for NFR devices
openFDA lists no recalls for product code NFR.
Frequently asked questions
What is FDA product code NFR?
NFR is the FDA product code for device, jaw tracking, for diagnosis of tmj / mpd disorders. It is a Class II device, regulated under 21 CFR 872.2060 and reviewed by the Dental panel.
What device class is NFR?
Class II, regulation 21 CFR 872.2060. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NFR
- Run a recall and safety report across every NFR manufacturer
- Watch product code NFR 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.