FDA product code MMT: Resin, Root Canal Filling Containing Chloroform
MMT is the FDA product code for resin, root canal filling containing chloroform. It is a Class III device, regulated under 21 CFR 872.3820 and reviewed by the Dental panel. Devices under MMT reach the market by PMA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Resin, Root Canal Filling Containing Chloroform |
| Device class | Class III |
| Regulation | 21 CFR 872.3820 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | PMA |
Recalls for MMT devices
openFDA lists no recalls for product code MMT.
Frequently asked questions
What is FDA product code MMT?
MMT is the FDA product code for resin, root canal filling containing chloroform. It is a Class III device, regulated under 21 CFR 872.3820 and reviewed by the Dental panel.
What device class is MMT?
Class III, regulation 21 CFR 872.3820. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MMT
- Run a recall and safety report across every MMT manufacturer
- Watch product code MMT 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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