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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 12 of 140
DeviceModel / ReferenceRegistriesClassStatus
Candulor TCR 600450
FDA UDI
Class IIActive
Candulor TCR 552280
FDA UDI
Class IIActive
Candulor TCR 616503
FDA UDI
Class IIActive
Candulor TCR 552915
FDA UDI
Class IIActive
Candulor TCR 698630
FDA UDI
Class IIActive
Candulor NFC+ 660219
FDA UDI
Class IIActive
Candulor TCR 552371
FDA UDI
Class IIActive
PhysioSelect TCR 696831
FDA UDI
Class IIActive
Candulor NFC+ 661250
FDA UDI
Class IIActive
Preference 578521
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661478
FDA UDI
Class IIActive
Aesthetic 611005
FDA UDI
Class IIUnknown
Candulor Preference 578277
FDA UDI
Class IIActive
Candulor TCR 552802
FDA UDI
Class IIActive
Candulor TCR 600433
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661468
FDA UDI
Class IIActive
Candulor TCR 697071
FDA UDI
Class IIActive
Candulor NFC+ 660272
FDA UDI
Class IIActive
Candulor TCR 552545
FDA UDI
Class IIActive
Candulor TCR 696882
FDA UDI
Class IIActive
Physioset TCR 6er 552594
FDA UDI
Class IIActive
Candulor TCR 697081
FDA UDI
Class IIActive
Candulor TCR 552832
FDA UDI
Class IIActive
Physioset Ct 547621
FDA UDI
Class IIUnknown
Physioset TCR 6er 552682
FDA UDI
Class IIActive
Candulor Preference 578591
FDA UDI
Class IIActive
Candulor TCR 552331
FDA UDI
Class IIActive
Candulor TCR 552821
FDA UDI
Class IIActive
Candulor TCR 552781
FDA UDI
Class IIActive
Candulor TCR 552870
FDA UDI
Class IIActive
Candulor NFC+ 641182
FDA UDI
Class IIActive
Candulor TCR 616486
FDA UDI
Class IIActive
Candulor NFC+ 660957
FDA UDI
Class IIActive
Candulor NFC+ 661106
FDA UDI
Class IIActive
Preference 578635
FDA UDI
Class IIActive
Preference 578473
FDA UDI
Class IIActive
PhysioSelect TCR 696801
FDA UDI
Class IIActive
Candulor TCR 757527
FDA UDI
Class IIActive
Preference 578517
FDA UDI
Class IIActive
Candulor TCR 757284
FDA UDI
Class IIActive
Preference 578355
FDA UDI
Class IIActive
Candulor TCR 698561
FDA UDI
Class IIActive
Candulor Preference 578451
FDA UDI
Class IIActive
PhysioStar NFC plus 6er 661241
FDA UDI
Class IIActive
Candulor TCR 696782
FDA UDI
Class IIActive
Candulor Preference 578344
FDA UDI
Class IIActive
Candulor Preference 578599
FDA UDI
Class IIActive
Candulor NFC+ 661453
FDA UDI
Class IIActive
Candulor NFC+ 661178
FDA UDI
Class IIActive
Candulor TCR 552752
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