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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 135 of 140
DeviceModel / ReferenceRegistriesClassStatus
Preference 578686
FDA UDI
Class IIActive
Candulor TCR 552590
FDA UDI
Class IIActive
BonSelect TCR 698607
FDA UDI
Class IIActive
Candulor Preference 578493
FDA UDI
Class IIActive
Preference 578379
FDA UDI
Class IIActive
Candulor TCR 552318
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660213
FDA UDI
Class IIActive
Physioset TCR 6er 552402
FDA UDI
Class IIActive
Physioset TCR 6er 600492
FDA UDI
Class IIActive
PhysioSelect TCR 696769
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660278
FDA UDI
Class IIActive
Physioset TCR 6er 552629
FDA UDI
Class IIActive
Bonartic TCR 8er 615250
FDA UDI
Class IIActive
Physioset TCR 6er 552232
FDA UDI
Class IIActive
Candulor Preference 578523
FDA UDI
Class IIActive
Candulor Preference 578724
FDA UDI
Class IIActive
Candulor TCR 552557
FDA UDI
Class IIActive
Candulor TCR 552573
FDA UDI
Class IIActive
Bonartic TCR 8er 600646
FDA UDI
Class IIActive
Candulor TCR 552327
FDA UDI
Class IIActive
Candulor TCR 600497
FDA UDI
Class IIActive
Physioset Ct 547422
FDA UDI
Class IIUnknown
CONDYLOFORM II NFCplus 660366
FDA UDI
Class IIActive
Physioset TCR 6er 552555
FDA UDI
Class IIActive
PhysioSelect TCR 696905
FDA UDI
Class IIActive
Candulor TCR 552205
FDA UDI
Class IIActive
Candulor TCR 600532
FDA UDI
Class IIActive
Aesthetic 676790
FDA UDI
Class IIUnknown
BONARTIC II NFCplus 660147
FDA UDI
Class IIActive
Physioset TCR 6er 552336
FDA UDI
Class IIActive
Preference 578297
FDA UDI
Class IIActive
Candulor TCR 757459
FDA UDI
Class IIActive
Candulor TCR 757297
FDA UDI
Class IIActive
Physioset TCR 6er 552212
FDA UDI
Class IIActive
Physioset TCR 6er 552707
FDA UDI
Class IIActive
Candulor TCR 757463
FDA UDI
Class IIActive
Physioset TCR 6er 600461
FDA UDI
Class IIActive
Candulor TCR 600442
FDA UDI
Class IIActive
Preference 605122
FDA UDI
Class IIActive
Candulor TCR 616513
FDA UDI
Class IIActive
Candulor TCR 757534
FDA UDI
Class IIActive
Candulor TCR 616487
FDA UDI
Class IIActive
Candulor TCR 698539
FDA UDI
Class IIActive
Candulor TCR 757338
FDA UDI
Class IIActive
Aesthetic 674556
FDA UDI
Class IIActive
Aesthetic 672693
FDA UDI
Class IIUnknown
Candulor TCR 616470
FDA UDI
Class IIActive
PhysioSelect TCR 696760
FDA UDI
Class IIActive
Preference 578703
FDA UDI
Class IIActive
Preference 578541
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