Facility

TALLADIUM, INC.

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	2023129
Establishment type	Manufacture Medical Device
Location	27360 WEST MUIRFIELD LN. Santa Clarita, CA, US 91355
Registration status	Active · expires 2026
Parent company	TALLADIUM, INC. (owner-operator 2023129)
Brand names	Luminesse PMMA; Luminesse Temporaries; Luminesse Acetal

Activity by year

Recalls (2)

Devices registered here (1)

Crown And Bridge, Temporary, Resin
Product code EBG (opens in a new tab) · Class II · Dental · 21 CFR 872.3770

Recalls & enforcement

Class IIITerminated2020-10-09
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 re…
Class IITerminated2020-08-06
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 line…

All facilities operated by TALLADIUM, INC.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “TALLADIUM, INC. (FEI 2023129) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2023129-talladium-inc/

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