Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Wright Health Group , Ltd.

US

Last updated May 23, 2026

What Wright Health Group , Ltd. makes

Wright Health Group, Ltd. manufactures resin artificial teeth, denture base resin kits, and dental casting non-noble alloys. These products include branded systems like Dentavit, Dentorium, Dentoluxx V, and Monarch, designed for dental prosthetics and restorative applications.

The company’s portfolio is regulated as Class II medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Wright Health Group, Ltd. manufacture?

Wright Health Group, Ltd. specializes in dental prosthetics and restorative materials. Their primary products include resin artificial teeth, denture base resin kits, and dental casting non-noble alloys. These materials are used in creating dental prosthetics, such as dentures, and are designed to provide durable, functional replacements for missing teeth or structures.

Where is Wright Health Group, Ltd. based?

The company is headquartered in the United States. This location influences its regulatory compliance, particularly with U.S. authorities like the FDA, which governs the classification and listing of its devices.

Which regulatory registries list Wright Health Group, Ltd.’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and patients to verify the identity and compliance status of specific devices.

How are Wright Health Group, Ltd.’s devices classified under medical device regulations?

All of Wright Health Group, Ltd.’s devices fall under Class II classification. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as resin-based dental prosthetics and alloys used in restorative dentistry.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
—

Catalogue (4309)

Page 86 of 87
DeviceModel / ReferenceRegistriesClassStatus
Dentoluxx V Anterior 1R Lower B3
FDA UDI
Class IIActive
Dentoluxx V Posterior 33L Lower C3
FDA UDI
Class IIActive
Dentoluxx V Anterior UY Upper C2
FDA UDI
Class IIActive
Dentoluxx V Anterior 1R Lower A1
FDA UDI
Class IIActive
Dentoluxx V Posterior PD Upper A3
FDA UDI
Class IIActive
Dentoluxx V Posterior PA Lower C2
FDA UDI
Class IIActive
Dentoluxx V Dentoluxx V Posterior 29Z Upper A3
FDA UDI
Class IIActive
Dentoluxx V Posterior 29M Upper C3
FDA UDI
Class IIActive
Dentoluxx V Anterior 1R Lower A4
FDA UDI
Class IIActive
Dentoluxx V Anterior 234 Upper C4
FDA UDI
Class IIActive
Dentoluxx V Anterior 1N Lower B4
FDA UDI
Class IIActive
Dentoluxx V Anterior 1N Lower C2
FDA UDI
Class IIActive
Dentoluxx V Anterior 2N Upper A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior 31L Upper A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior PB Upper A3
FDA UDI
Class IIActive
Dentoluxx V Anterior 266 Upper C2
FDA UDI
Class IIActive
Dentoluxx V Posterior 33L Lower A1
FDA UDI
Class IIActive
Dentoluxx V Posterior 31Z Upper B2
FDA UDI
Class IIActive
Dentoluxx V Anterior 4H Upper A2
FDA UDI
Class IIActive
Dentoluxx V Posterior PB Upper A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior 31Z Lower A4
FDA UDI
Class IIActive
Dentoluxx V Anterior 3R Upper A1
FDA UDI
Class IIActive
Dentoluxx V Anterior 3P Upper D3
FDA UDI
Class IIActive
Dentoluxx V Posterior 31Z Upper B4
FDA UDI
Class IIActive
Dentoluxx V Anterior 2P Lower B2
FDA UDI
Class IIActive
Dentoluxx V Posterior PBS Lower B2
FDA UDI
Class IIActive
Dentoluxx V Posterior PC Upper A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior 31L Upper A3
FDA UDI
Class IIActive
Dentoluxx V Anterior 3N Upper A4
FDA UDI
Class IIActive
Dentoluxx V Posterior 33L Upper A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior 31M Upper A2
FDA UDI
Class IIActive
Dentoluxx V Anterior 264 Upper D2
FDA UDI
Class IIActive
Dentoluxx V Anterior 25 Lower D2
FDA UDI
Class IIActive
Dentoluxx V Anterior 154 Upper B1
FDA UDI
Class IIActive
Dentoluxx V Anterior 5P Upper B4
FDA UDI
Class IIActive
Dentoluxx V Anterior 324 Upper C1
FDA UDI
Class IIActive
Dentoluxx V Posterior PC Upper D4
FDA UDI
Class IIActive
Dentoluxx V Posterior 31M Lower C2
FDA UDI
Class IIActive
Dentoluxx V Posterior 31RF Lower B1
FDA UDI
Class IIActive
Dentoluxx V Posterior 33L Upper B1
FDA UDI
Class IIActive
Dentoluxx V Posterior 31M Upper D2
FDA UDI
Class IIActive
Dentoluxx V Anterior UY Upper BL
FDA UDI
Class IIActive
Dentoluxx V Anterior 1R Lower A3.5
FDA UDI
Class IIActive
Dentoluxx V Posterior PB Lower A2
FDA UDI
Class IIActive
Dentoluxx V Anterior 2P Upper BL
FDA UDI
Class IIActive
Dentoluxx V Anterior 3C Lower D4
FDA UDI
Class IIActive
Dentoluxx V Posterior 31L Upper B4
FDA UDI
Class IIActive
Dentoluxx V Posterior 29M Lower A1
FDA UDI
Class IIActive
Dentoluxx V Anterior 264 Upper C3
FDA UDI
Class IIActive
Dentoluxx V Posterior PC Upper A2
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Wright Health Group Dundee Dundee City · GB FEI 3003103749