FDA product code NVG: Tissue Culture, Accessories, Dental
NVG is the FDA product code for tissue culture, accessories, dental. It is a Class I device, regulated under 21 CFR 864.2240 and reviewed by the Hematology panel. Devices under NVG reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
Intended to temporarilty nourish cells on an avulsed tooth
Classification
| Field | Value |
|---|---|
| Device name | Tissue Culture, Accessories, Dental |
| Device class | Class I |
| Regulation | 21 CFR 864.2240 |
| Review panel | HE — Hematology |
| Medical specialty | Hematology |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for NVG devices
openFDA lists no recalls for product code NVG.
Frequently asked questions
What is FDA product code NVG?
NVG is the FDA product code for tissue culture, accessories, dental. It is a Class I device, regulated under 21 CFR 864.2240 and reviewed by the Hematology panel.
What device class is NVG?
Class I, regulation 21 CFR 864.2240. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code NVG
- Run a recall and safety report across every NVG manufacturer
- Watch product code NVG 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.