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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 138 of 140
DeviceModel / ReferenceRegistriesClassStatus
Bonartic TCR 8er 552839
FDA UDI
Class IIActive
Preference 578311
FDA UDI
Class IIActive
Physioset TCR 6er 616495
FDA UDI
Class IIActive
Bonartic TCR 8er 552829
FDA UDI
Class IIActive
BONARTIC II NFCplus 660139
FDA UDI
Class IIActive
BONARTIC II NFCplus 643067
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661242
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661080
FDA UDI
Class IIActive
Physioset TCR 6er 552621
FDA UDI
Class IIActive
Physioset TCR 6er 552540
FDA UDI
Class IIActive
Physioset TCR 6er 600441
FDA UDI
Class IIActive
Bonartic TCR 8er 600603
FDA UDI
Class IIActive
Physioset TCR 6er 600522
FDA UDI
Class IIActive
Bonartic TCR 8er 600620
FDA UDI
Class IIActive
Candulor TCR 757511
FDA UDI
Class IIActive
Candulor TCR 757430
FDA UDI
Class IIActive
Bonartic Ct 548150
FDA UDI
Class IIUnknown
Candulor TCR 698625
FDA UDI
Class IIActive
Candulor TCR 552841
FDA UDI
Class IIActive
Bonartic TCR 8er 552824
FDA UDI
Class IIActive
Candulor Preference 605151
FDA UDI
Class IIActive
Candulor TCR 552605
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661084
FDA UDI
Class IIActive
Candulor TCR 757547
FDA UDI
Class IIActive
Preference 578456
FDA UDI
Class IIActive
Candulor TCR 757277
FDA UDI
Class IIActive
Candulor Preference 578264
FDA UDI
Class IIActive
Preference 578338
FDA UDI
Class IIActive
Candulor TCR 757267
FDA UDI
Class IIActive
Candulor TCR 696809
FDA UDI
Class IIActive
Candulor TCR 552920
FDA UDI
Class IIActive
Candulor TCR 600551
FDA UDI
Class IIActive
Candulor TCR 600462
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660312
FDA UDI
Class IIActive
Bonartic TCR 8er 600591
FDA UDI
Class IIActive
Candulor TCR 757475
FDA UDI
Class IIActive
Preference 578627
FDA UDI
Class IIActive
Candulor TCR 615256
FDA UDI
Class IIActive
Candulor Preference 578341
FDA UDI
Class IIActive
Candulor TCR 696789
FDA UDI
Class IIActive
Aesthetic 672709
FDA UDI
Class IIUnknown
PHYSIOSTAR NFCplus 660964
FDA UDI
Class IIActive
Aesthetic Red 672714
FDA UDI
Class IIActive
Candulor TCR 696874
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661295
FDA UDI
Class IIActive
Bonartic Ct 548057
FDA UDI
Class IIUnknown
Candulor TCR 757310
FDA UDI
Class IIActive
PHYSIOSTAR NFCplus 661088
FDA UDI
Class IIActive
CONDYLOFORM II NFCplus 660265
FDA UDI
Class IIActive
Condyloform Ct 562093
FDA UDI
Class IIUnknown

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