TALLADIUM, INC.

FDA Device Registration & Listing · Santa Clarita, CA, US · Registration 2023129

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2023129
FEI Number
2023129
Entity Name
TALLADIUM, INC.
City/State/Country
Santa Clarita, CA, US
Establishment Address
27360 WEST MUIRFIELD LN., Santa Clarita, CA 91355, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TALLADIUM, INC. (Owner Number: 2023129)
Owner / Operator Contact Address
27360 WEST MUIRFIELD LN., --, Valencia, CA 91355, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Luminesse PMMA Luminesse Acetal Luminesse Temporaries Luminesse Porcelain System Luminesse Titanium Discs Luminesse Chrome-Cobalt Discs Tilite-Chrome Post Solder Hi-Tech Pre-Solder Laser Welding wire Luminesse Multilayer Anterior Zirconia AT Luminesse Anterior Zirconia AT Luminesse Shaded Anterior Zirconia AT Luminesse Shaded Zirconia SZ Luminesse Pre-Sintered Zirconia Coloring Liquid

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBG Crown And Bridge, Temporary, Resin Dental Class 2 872.3770 2015-04-29
EIH Powder, Porcelain Dental Class 2 872.6660 2015-05-13
EJH Alloy, Metal, Base Dental Class 2 872.3710 2014-06-17
EIH Powder, Porcelain Dental Class 2 872.6660 2017-08-28
EIH Powder, Porcelain Dental Class 2 872.6660 2019-01-28
EIH Powder, Porcelain Dental Class 2 872.6660 2015-07-02

Official Correspondent

Eddie HARMS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TALLADIUM, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K143656 H.C. Starck Ceramics GmbH StarCeram® Z-Nature, StarCeram® Z-Smile 2015-07-09
K810521 C.Vaupel Dental, Inc. CO-SPAN 13.5 CASTING ALLOY 1981-03-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0017-2017 Ivoclar Vivadent, Inc. 2
Zenostar MT Color Impulse blue, Art. no. 681165 Product Usage: For coloring dental porcelain
Z-0018-2017 Ivoclar Vivadent, Inc. 2
Zenostar MT Color Impulse brown, art. no. 681169 Product Usage: For coloring dental porcelain
Z-0019-2017 Ivoclar Vivadent, Inc. 2
Zenostar MT Color Impulse grey, art. no. 681167 Product Usage: For coloring dental porcelain
Z-0020-2017 Ivoclar Vivadent, Inc. 2
Zenostar MT Color Impulse violet, art. no. 681166 Product Usage: For coloring dental porcelain
Z-0021-2017 Ivoclar Vivadent, Inc. 2
Zenostar MT Color A1 60ml, art. no. 681050, Product Usage: For coloring dental porcelain

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2023129. Last updated year: 2026. Please use registration number 2023129 when referencing this establishment in official correspondence.
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