FDA product code DZG: Suture, Dental
DZG is the FDA product code for suture, dental. It is a Class III device, reviewed by the General and Plastic Surgery panel. Devices under DZG reach the market by PMA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Suture, Dental |
| Device class | Class III |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | PMA |
| Implant | Yes |
Recalls for DZG devices
openFDA lists no recalls for product code DZG.
Frequently asked questions
What is FDA product code DZG?
DZG is the FDA product code for suture, dental. It is a Class III device, reviewed by the General and Plastic Surgery panel.
What device class is DZG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code DZG
- Run a recall and safety report across every DZG manufacturer
- Watch product code DZG 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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