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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 132 of 140
DeviceModel / ReferenceRegistriesClassStatus
Physioset TCR 6er 552627
FDA UDI
Class IIActive
Physioset TCR 6er 552384
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661336
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660283
FDA UDI
Class IIActive
Physioset TCR 6er 552462
FDA UDI
Class IIActive
Bonartic TCR 8er 552800
FDA UDI
Class IIActive
Candulor TCR 552228
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661411
FDA UDI
Class IIActive
Preference 578359
FDA UDI
Class IIActive
Candulor TCR 616490
FDA UDI
Class IIActive
Candulor TCR 552267
FDA UDI
Class IIActive
Candulor TCR 698542
FDA UDI
Class IIActive
Bonartic TCR 8er 552898
FDA UDI
Class IIActive
Candulor TCR 552316
FDA UDI
Class IIActive
Candulor Preference 578575
FDA UDI
Class IIActive
Candulor TCR 552425
FDA UDI
Class IIActive
Candulor TCR 757264
FDA UDI
Class IIActive
Physioset TCR 6er 600424
FDA UDI
Class IIActive
Candulor TCR 600469
FDA UDI
Class IIActive
Physioset Ct 547369
FDA UDI
Class IIUnknown
PHYSIOSTAR NFCplus 660928
FDA UDI
Class IIActive
Preference 578322
FDA UDI
Class IIActive
Aesthetic Wax 662471
FDA UDI
Class IActive
Bonartic Ct 548180
FDA UDI
Class IIUnknown
PhysioSelect TCR 696879
FDA UDI
Class IIActive
Physioset TCR 6er 552201
FDA UDI
Class IIActive
Candulor TCR 616457
FDA UDI
Class IIActive
PhysioSelect TCR 696979
FDA UDI
Class IIActive
Candulor TCR 552913
FDA UDI
Class IIActive
Candulor TCR 698560
FDA UDI
Class IIActive
PhysioSelect TCR 697003
FDA UDI
Class IIActive
Candulor TCR 552635
FDA UDI
Class IIActive
Candulor TCR 552724
FDA UDI
Class IIActive
Physioset Ct 547615
FDA UDI
Class IIUnknown
Candulor TCR 696880
FDA UDI
Class IIActive
Candulor Preference 578715
FDA UDI
Class IIActive
Candulor TCR 552726
FDA UDI
Class IIActive
Candulor TCR 552637
FDA UDI
Class IIActive
Aesthetic 611009
FDA UDI
Class IIUnknown
Preference 578373
FDA UDI
Class IIActive
Bonartic TCR 8er 552903
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660380
FDA UDI
Class IIActive
PhysioSelect TCR 697055
FDA UDI
Class IIActive
Preference 578633
FDA UDI
Class IIActive
Preference 578380
FDA UDI
Class IIActive
PhysioSelect TCR 697028
FDA UDI
Class IIActive
Physioset Ct 547559
FDA UDI
Class IIUnknown
BonSelect TCR 698548
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661308
FDA UDI
Class IIActive
BONARTIC II NFCplus 660174
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