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Sign in to claim this brandDANVILLE MATERIALS, LLC
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- xxx.xxx
- —
- —
- [email protected]
- Phone
- +1(760)743-7744
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 601302743
Catalogue (260)
Page 6 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| DMRC Light Cure Orthodontic Adhesive System | K142880 | FDA 510(k) | Class II | Active |
| Starfill 2b Hv (high Viscosity) Rockcore, Model: 90838 And Starfill 2b Lv (low Viscosity), Model: 90150 | K092912 | FDA 510(k) | Class II | Active |
| Snowpost, Snowlight | K012354 | FDA 510(k) | Class I | Active |
| Dmrc Nanoflow Dmrc Nanocomposite Ebond Sure Etch Gel Sure Etch Liquid | K121880 | FDA 510(k) | Class II | Active |
| Turbo Temp 3 | K102753 | FDA 510(k) | Class II | Active |
| Prelude One | K090106 | FDA 510(k) | Class II | Active |
| Prelude | K040952 | FDA 510(k) | Class II | Active |
| Star+ VPS Scannable Impression Material | K152349 | FDA 510(k) | Class II | Active |
| DMRC Self-Cure Bracket Adhesive One Step and Primer | K142886 | FDA 510(k) | Class II | Active |
| DMRC Dual Cure Orthodontic Band Cement | K142881 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jun 24, 2016 | Z-2530-2016 | — | terminated | The Perioscopy Sheaths are currently provided with a label that indicates the Sheath has a 3 year shelf-life/expiry date. Danville Materials has become aware that validation data are not available to support the 3-year shelf-life/expiration dating claim. |