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UNION DENTAL SA

US

Last updated May 23, 2026

What UNION DENTAL SA makes

Union Dental SA manufactures temporary dental crowns and bridges, as well as resin-based artificial teeth for dental prosthetics. Their product line includes polymethyl methacrylate (PMMA) resin systems for dental restorations, designed for short-term use in patient care.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates within the United States regulatory framework for dental materials and restorative products.

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

Frequently asked questions

What types of dental devices does Union Dental SA manufacture?

Union Dental SA specializes in temporary dental crowns and bridges, as well as resin artificial teeth for dental prosthetics. Their products include polymethyl methacrylate (PMMA) resin systems, which are primarily used for short-term dental restorations. These devices are designed to provide functional and aesthetic solutions during transitional phases of dental treatment.

Where is Union Dental SA based, and under which regulatory framework do their devices operate?

Union Dental SA is based in the United States. Their devices operate under the U.S. regulatory framework, specifically adhering to FDA guidelines. Since their products fall under Class II classification, they are subject to FDA requirements for moderate-risk medical devices, including registration, listing, and compliance with quality system regulations.

Are Union Dental SA’s devices listed in any regulatory registries, and if so, which ones?

Yes, Union Dental SA’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 other stakeholders to identify and verify the devices through a standardized identification system.

How are Union Dental SA’s devices classified under FDA regulations?

Union Dental SA’s devices are classified as Class II under FDA regulations. This classification is assigned based on the level of control needed to ensure the device’s safety and effectiveness. Class II devices generally require special controls in addition to general controls (like good manufacturing practices) to mitigate potential risks, such as those associated with temporary restorations or resin-based dental materials.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
462114760

Catalogue (3322)

Page 67 of 67
DeviceModel / ReferenceRegistriesClassStatus
10temp DISC C2 10 LAYERS 98,5/25mm
EUDAMEDFDA UDI
Class IIActive
Eledent POSTERIOR TEETH C1/34MI
FDA UDI
Class IIActive
Anaxdent Pmma Z MULTI BLANK B1 98,5/12mm
FDA UDI
Class IIActive
Anaxdent Pmma Z Monolayer BLANK B1 95/25mm
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH C4/30MS
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH C1/29MS
FDA UDI
Class IIActive
Anaxdent Pmma U MULTIBLANK B2 98,5/20mm
FDA UDI
Class IIActive
Anaxdent Pmma U Monolayer BLANK A2 98,5/20mm
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH A3/31LI
FDA UDI
Class IIActive
Anaxdent Pmma Z MULTI BLANK B0 95/16mm
FDA UDI
Class IIActive
Anaxdent Pmma Z Monolayer BLANK A2 95/25mm
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH B3/33MI
FDA UDI
Class IIActive
Anaxdent Pmma U MULTI BLANK A3 98,5/12mm
FDA UDI
Class IIActive
Eledent ANTERIOR TEETH C4/E13
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH C4/33MI
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH D2/30FI
FDA UDI
Class IIActive
Anaxdent Pmma Z MULTI BLANK A1 95/16mm
FDA UDI
Class IIActive
10temp DISC B3 10 LAYERS 98,5/20mm
EUDAMEDFDA UDI
Class IIActive
Anaxdent Pmma Blank PMMA MULTI Blank AG A2 20mm
FDA UDI
Class IIUnknown
Eledent POSTERIOR TEETH A4/29MI
FDA UDI
Class IIActive
Eledent POSTERIOR TEETH B3/29MI
EUDAMEDFDA UDI
Class IIActive
Eledent ANTERIOR TEETH B0/E13
FDA UDI
Class IIActive

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