FDA product code NSK: Dentures, Partial
NSK is the FDA product code for dentures, partial. It is a Not classified device, reviewed by the Dental panel. Devices under NSK reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
Foreign dental lab manufactured partial dentures are manufactured as finished products from denture resins and other supporting materials.
Classification
| Field | Value |
|---|---|
| Device name | Dentures, Partial |
| Device class | Not classified |
| Review panel | DE — Dental |
| Medical specialty | Unknown |
| Premarket route | 510(k) exempt |
Recalls for NSK devices
openFDA lists no recalls for product code NSK.
Frequently asked questions
What is FDA product code NSK?
NSK is the FDA product code for dentures, partial. It is a Not classified device, reviewed by the Dental panel.
What device class is NSK?
Not classified. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code NSK
- Run a recall and safety report across every NSK manufacturer
- Watch product code NSK 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.