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Sign in to claim this brandTALLADIUM, INC.
US
Last updated September 17, 2026
What TALLADIUM, INC. makes
Talladium, Inc. produces dental materials for appliance fabrication, including ceramic-based zirconia blocks and polymer-based PMMA discs for dental prosthetics. Their portfolio includes dental casting alloys—both noble and non-noble—along with specialized powders, modifiers, and dyes for dentin, incisal layers, and multilayer anterior restorations. The company also supplies materials for soldering and pre-shaded dental models to enhance aesthetic outcomes in restorative dentistry.
All listed devices fall under Class II regulatory classification in the U.S. and are recorded in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. medical device regulations.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- 27360 WEST MUIRFIELD LN., Santa Clarita, CA, 91355
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2023129
- DUNS Number
- 094430642
Catalogue (1101)
Page 18 of 23| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tilite Ceramic Alloys - Omega | 111-5 | FDA UDI | Class II | Active |
| Luminesse Low Fusing Incisal | 19031 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5147B1 | FDA UDI | Class II | Active |
| Luminesse Low Fusing Porcelain | 1900ST150 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5172 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5081MLA1A2HT | FDA UDI | Class II | Active |
| Luminesse ZR Dentin Powder | 1972C2 | FDA UDI | Class II | Active |
| Luminesse HF Opacious Dentins | 1962B3 | FDA UDI | Class II | Active |
| Luminesse Zirconia Blocks | 5162C1 | FDA UDI | Class II | Active |
| Luminesse Zirconia Blocks | 5091HS | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 4302A0 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 5320B2 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5143NR | FDA UDI | Class II | Active |
| Luminesse Zirconia Blocks | 5137 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5143B1 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 5320A4 | FDA UDI | Class II | Active |
| Color Liquid | 25216 | FDA UDI | Class II | Active |
| Luminesse Shaded PMMA Discs | 5301B1 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5147ATV4 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 4301B3 | FDA UDI | Class II | Active |
| Luminesse Shaded PMMA Discs | 5301A1 | FDA UDI | Class II | Active |
| Luminesse LF Opaque Powder | 1913B4 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 6849-A2 | FDA UDI | Class II | Active |
| Luminesse Zirconia Blocks | 5099 | FDA UDI | Class II | Active |
| Color Liquid | 25217 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5144ATV5 | FDA UDI | Class II | Active |
| Luminesse HF Gingivals | 1961LF | FDA UDI | Class II | Active |
| Luminesse HF Dentin Powder | 1952B3 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5143D3 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5143ATV1 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5143C3 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 4303A35 | FDA UDI | Class II | Active |
| Luminesse ZR Dentin Powder | 1972A2 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5178HTT | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 5320D4 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 5320A35 | FDA UDI | Class II | Active |
| Luminesse Zirconia Blocks | 5168 | FDA UDI | Class II | Active |
| Luminesse Universal Glaze Powder | 1954-UG | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5181AT | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 19814-OFAML-A2 | FDA UDI | Class II | Active |
| Luminesse Ti-Cam Discs | 20171 | FDA UDI | Class II | Active |
| Luminesse Multi-Layer PMMA Discs | 5336B2 | FDA UDI | Class II | Active |
| Luminesse Shaded PMMA Discs | 5307C3 | FDA UDI | Class II | Active |
| Luminesse Zirconia Discs | 5144D2 | FDA UDI | Class II | Active |
| Luminesse Ti-Cam Discs | 20168 | FDA UDI | Class II | Active |
| Luminesse Shaded PMMA Discs | 5301B4 | FDA UDI | Class II | Active |
| Color Liquid | 25211 | FDA UDI | Class II | Active |
| Luminesse HF Opaque Powder | 1963D2 | FDA UDI | Class II | Active |
| Luminesse HF Incisal | 1953C | FDA UDI | Class II | Active |
| Color Liquid | 25209 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Talladium, Inc. has two recall records, both initiated in 2020—one on August 6 and the other on October 9—with both currently marked as terminated. The recalls involved labeling inaccuracies: one concerned incorrect linear shrinkage values on zirconia blank discs, where the stated shrinkage rate fell outside the acceptable range of 1.225 to 1.275, and the other involved mislabeled heat-cured polymethylmethacrylate (PMMA) milling blanks, where the product inside did not match the label’s specified part number.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 9, 2020 | Z-0512-2021 | — | terminated | Heat-cured polymethylmethacrylate (PMMA) milling blank product used to make long-term temporary crowns and bridge restorations has incorrect label. label states Part no. 5336-B1 (98x20mm). However, the item inside the box was Part no. 4302-B1 (95x20mm). An incorrect label may result in compatibility issues when setting up the disc with milling machine fixtures due to size variation. |
| Aug 6, 2020 | Z-2943-2020 | — | terminated | The linear shrinkage on the zirconia blank disc s part label is incorrect. The average linear shrinkage found on the product label was outside the acceptable range. The acceptable average linear shrinkage ranges between 1.225 to 1.275. The production lot being recalled has a linear shrinkage rate of 2.251 which is above the acceptable range. |