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TALLADIUM, INC.

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: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2023129
DUNS Number: 094430642

Catalogue (1101)

Page 21 of 23

Device	Model / Reference	Registries	Class	Status
Luminesse Shaded PMMA Discs	5308-A4	FDA UDI	Class II	Active
Luminesse Clear PMMA Discs	5213Z	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5144A4	FDA UDI	Class II	Active
Luminesse Shaded PMMA Discs	5298A35	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5147ATV5	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5171ATV2	FDA UDI	Class II	Active
Luminesse HF Opacious Dentins	1962B4	FDA UDI	Class II	Active
Luminesse HF Opacious Dentins	1962A4	FDA UDI	Class II	Active
Luminesse LF Opacious Dentin	1912A1	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5148B4	FDA UDI	Class II	Active
Luminesse Zirconia Blocks	5162C2	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5144MLA1A2HT	FDA UDI	Class II	Active
Luminesse ZR Dentin Powder	1972C4	FDA UDI	Class II	Active
Luminesse Low Fusing Dentin Powder	1902A1	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5176	FDA UDI	Class II	Active
Luminesse ZR Incisal	1973B	FDA UDI	Class II	Active
Luminesse Ti-Cam Discs	5254	FDA UDI	Class II	Active
Luminesse Shaded PMMA Discs	5298B1	FDA UDI	Class II	Active
Luminesse HF Dentin Powder	1952A0	FDA UDI	Class II	Active
Luminesse Low Fusing Porcelain	1900C250	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5145ATV2	FDA UDI	Class II	Active
Luminesse Zirconia Discs	19816-ATML-D2	FDA UDI	Class II	Active
Luminesse ZR Dentin Powder	1972D3	FDA UDI	Class II	Active
Luminesse Shaded PMMA Discs	5308D2	FDA UDI	Class II	Active
Luminesse Zirconia Blocks	5091	FDA UDI	Class II	Active
Luminesse ZR Trial Kit	1972T	FDA UDI	Class II	Active
Luminesse Zirconia Blocks	5089HS	FDA UDI	Class II	Active
Luminesse Ti-Cam Discs	5239	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5147C3	FDA UDI	Class II	Active
Luminesse ZR Incisal	19734	FDA UDI	Class II	Active
Luminesse LF Opaque Powder	1913C1	FDA UDI	Class II	Active
Luminesse Multilayer Anterior Zirconia AT	19814-ATML-D3	FDA UDI	Class II	Active
Luminesse ZR Dentin Modifiers	1978Y	FDA UDI	Class II	Active
Luminesse Zirconia Blocks	5118HS	FDA UDI	Class II	Active
Luminesse Shaded PMMA Discs	5300B3	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5185HTT	FDA UDI	Class II	Active
Luminesse ZR Margin	1979M3	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5144MLA3A35HT	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5143C4	FDA UDI	Class II	Active
Luminesse Zirconia Discs	5143A4	FDA UDI	Class II	Active
Luminesse Zirconia Discs	19518-OFA	FDA UDI	Class II	Active
Luminesse Low Fusing Incisal	19033	FDA UDI	Class II	Active
Tilite Ceramic Alloys - Star	102-5	FDA UDI	Class II	Active
Luminesse Shaded PMMA Discs	5301A0	FDA UDI	Class II	Active
Color Liquid	25230	FDA UDI	Class II	Active
Luminesse HF Opacious Dentins	1962C4	FDA UDI	Class II	Active
Luminesse LF Dentin Powder	1908MBR	FDA UDI	Class II	Active
Luminesse Zirconia Discs	19814-OFAML-D2	FDA UDI	Class II	Active
Luminesse HF Dentin Powder	1952A1	FDA UDI	Class II	Active
Luminesse Low Fusing Porcelain	1900A350	FDA UDI	Class II	Active

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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.