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Candulor AG

US

Last updated May 23, 2026

What Candulor AG makes

Candulor AG manufactures dental materials used in prosthetic and orthodontic applications, including resin-based artificial teeth, denture base resins, dental appliance fabrication resins, and custom dental impression tray materials. Their product line includes kits and specialized resins designed for precision fitting and durability in dental prosthetics, such as removable dentures and orthodontic appliances.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Candulor AG operates from the United States, adhering to regulatory requirements for dental materials and prosthetics in that jurisdiction.

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 Candulor AG manufacture?

Candulor AG specializes in dental materials used primarily for prosthetic and orthodontic applications. Their product line includes resin-based artificial teeth, denture base resin kits, dental appliance fabrication materials, and custom dental impression tray materials. These materials are designed for precision fitting and durability in dental prosthetics, such as removable dentures and orthodontic appliances.

Where is Candulor AG based, and what regulatory jurisdiction does it operate under?

Candulor AG is based in the United States. As a manufacturer, it operates under the regulatory requirements of the FDA, ensuring its dental materials comply with U.S. standards for safety, performance, and quality in prosthetic and orthodontic applications.

Which regulatory registries or databases list Candulor AG’s devices?

Candulor AG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are Candulor AG’s devices classified under FDA regulations?

Candulor AG’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with.

What is the primary purpose of the dental materials produced by Candulor AG?

The primary purpose of Candulor AG’s dental materials is to support the fabrication of durable, well-fitting dental prosthetics and orthodontic appliances. Their resin-based products, such as artificial teeth and denture base resins, are engineered to provide stability, longevity, and a natural appearance in restorative dental work, ensuring patient comfort and functionality.

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
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DUNS Number
480467422

Catalogue (6988)

Page 129 of 140
DeviceModel / ReferenceRegistriesClassStatus
Physioset TCR 6er 552309
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661045
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660215
FDA UDI
Class IIActive
Physioset TCR 6er 552323
FDA UDI
Class IIActive
BONARTIC II NFCplus 660144
FDA UDI
Class IIActive
Candulor TCR 552528
FDA UDI
Class IIActive
Candulor TCR 696937
FDA UDI
Class IIActive
BonSelect TCR 698660
FDA UDI
Class IIActive
Physioset TCR 6er 552196
FDA UDI
Class IIActive
Candulor TCR 696830
FDA UDI
Class IIActive
PhysioStar NFC plus 6er 661148
FDA UDI
Class IIActive
Preference 578655
FDA UDI
Class IIActive
Condyloform Ct 548499
FDA UDI
Class IIUnknown
BonSelect TCR 698584
FDA UDI
Class IIActive
Preference 578599
FDA UDI
Class IIActive
Candulor TCR 757493
FDA UDI
Class IIActive
Preference 578564
FDA UDI
Class IIActive
Candulor TCR 552226
FDA UDI
Class IIActive
Candulor TCR 553438
FDA UDI
Class IIActive
Candulor TCR 697098
FDA UDI
Class IIActive
Candulor TCR 552884
FDA UDI
Class IIActive
Candulor TCR 698531
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660247
FDA UDI
Class IIActive
BONARTIC II NFCplus 660166
FDA UDI
Class IIActive
Physioset TCR 6er 552355
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661072
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661314
FDA UDI
Class IIActive
Candulor TCR 552481
FDA UDI
Class IIActive
Preference 578668
FDA UDI
Class IIActive
Preference 578596
FDA UDI
Class IIActive
Candulor TCR 698633
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660332
FDA UDI
Class IIActive
Preference 578692
FDA UDI
Class IIActive
Physioset TCR 6er 552410
FDA UDI
Class IIActive
Physioset TCR 6er 552600
FDA UDI
Class IIActive
Candulor TCR 696783
FDA UDI
Class IIActive
Physioset TCR 6er 552400
FDA UDI
Class IIActive
Candulor TCR 696750
FDA UDI
Class IIActive
Bonartic TCR 8er 600609
FDA UDI
Class IIActive
Physioset TCR 6er 600437
FDA UDI
Class IIActive
Bonartic TCR 8er 552896
FDA UDI
Class IIActive
Bonartic Ct 548158
FDA UDI
Class IIUnknown
Physioset Ct 547493
FDA UDI
Class IIUnknown
Candulor TCR 757506
FDA UDI
Class IIActive
Candulor TCR 757540
FDA UDI
Class IIActive
Candulor TCR 553435
FDA UDI
Class IIActive
Candulor Preference 578726
FDA UDI
Class IIActive
Physioset TCR 6er 552364
FDA UDI
Class IIActive
Candulor TCR 552796
FDA UDI
Class IIActive
Candulor TCR 697054
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.

  • Candulor, Ag Glattpark Zurich · CH FEI 1000277456