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Dentorium

FDA UDI

Class II (US FDA UDI)

by Wright Health Group , Ltd.

Identity

Trade Name
Dentorium FDA UDI
Generic Name
Dental casting non-noble alloy FDA UDI
Device Name
Bonding Alloy FDA UDI
Model / Reference
Chrome Cobalt Neutral Ingot Hard No3 per FDA UDI
Description
Bonding Alloy FDA UDI

Identifiers

Catalog Number
AL123KG FDA UDI
Primary DI / UDI-DI
05056079040626 FDA UDI
FDA Product Code
EJH FDA UDI
GMDN Term
Dental casting non-noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3710 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental casting non-noble alloy

Dentorium by Wright Health Group , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting non-noble alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02f24dfd-6b90-48d7-8e50-3f9d33d5aca0 35 fields · synced Jun 8, 2026