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Dentsply Professional

US

Last updated May 24, 2026

What Dentsply Professional makes

Dentsply Professional manufactures ceramic materials for dental appliance fabrication, including high-strength dental ceramics like Ceramco 3, used in crowns, bridges, and other restorative applications. Their portfolio also includes ultrasonic dental scaling systems, such as the Cavitron®, along with specialized handpiece tips for periodontal debridement and single-use polishing cups for dental procedures. Additional products include dental cavity varnishes, irrigation handpieces for delivery systems, and resin-based artificial teeth like Lucitone Digital IPN 3D Premium Tooth.

The company’s devices are regulated under the FDA’s classification system, with products falling into Class I and Class II categories. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The manufacturer operates from the United States.

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 Dentsply Professional manufacture?

Dentsply Professional specializes in dental devices, primarily focusing on materials and systems for restorative and cleaning procedures. Their portfolio includes high-strength ceramic materials like Ceramco 3 for dental appliance fabrication (such as crowns and bridges), ultrasonic dental scaling systems like Cavitron® for plaque removal, periodontal handpiece tips, single-use polishing cups, dental cavity varnishes, irrigation handpieces, and resin-based artificial teeth like Lucitone Digital IPN 3D Premium Tooth. These products cater to both restorative and hygiene needs in dentistry.

Where is Dentsply Professional based, and how does that affect its devices?

Dentsply Professional is headquartered in the United States, which means its devices are subject to U.S. regulatory requirements, including FDA oversight. Since the company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, they comply with U.S. traceability and compliance standards for medical devices. This ensures their devices meet the necessary regulatory criteria for distribution and use in the American market.

Which regulatory registries list Dentsply Professional’s devices?

Dentsply Professional’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product code to each device, enabling better tracking, transparency, and compliance with U.S. medical device regulations. This registry helps healthcare providers and regulators verify device details, such as manufacturer information and classification.

How are Dentsply Professional’s devices classified under U.S. regulations?

Dentsply Professional’s devices fall into two main FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and regulatory history, ensuring appropriate oversight for each product.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(800)243-1942
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
144140845

Catalogue (526)

Page 1 of 11
DeviceModel / ReferenceRegistriesClassStatus
Nupro® 965068
FDA UDI
Class IActive
Ceramco 3 303910
FDA UDI
Class IIActive
Ceramco 3 305162
FDA UDI
Class IIActive
Ceramco 3 305913
FDA UDI
Class IIActive
Nupro® 965773
FDA UDI
Class IActive
Ceramco 3 305405
FDA UDI
Class IIActive
Ceramco 3 305166
FDA UDI
Class IIActive
Ceramco 3 303140
FDA UDI
Class IIActive
Nupro 90741L03
FDA UDI
Class IIActive
Cavitron® 80395
FDA UDI
Class IIActive
Ceramco 3 305110
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906390
FDA UDI
Class IIActive
Sani-Tip® 122214
FDA UDI
Class IActive
Nupro® 965750
FDA UDI
Class IActive
Ceramco 3 303130
FDA UDI
Class IIActive
Nupro® 965069
FDA UDI
Class IActive
Cavitron® 8129502
FDA UDI
Class IIUnknown
Lucitone Digital IPN 3D Premium Tooth 906381
FDA UDI
Class IIActive
Cavitron® 8800501
FDA UDI
Class IIActive
Ceramco 3 303610
FDA UDI
Class IIActive
Nupro® 130227
FDA UDI
Class IIActive
Sani-Tip® 122280N
FDA UDI
Class IActive
Ceramco 3 305110
FDA UDI
Class IIActive
Cavitron® 8800003
FDA UDI
Class IIActive
Cavitron® 81295
FDA UDI
Class IIActive
Ceramco 3 305221
FDA UDI
Class IIActive
Ceramco 3 305113
FDA UDI
Class IIActive
Sani-Shield® 130010
FDA UDI
Class IIActive
Sani-Tip® 122224
FDA UDI
Class IActive
Ceramco 3 305204
FDA UDI
Class IIActive
Cavitron® 79292
FDA UDI
Class IIActive
Cavitron® 8800204
FDA UDI
Class IIActive
Nupro® 965766
FDA UDI
Class IActive
Ceramco 3 305100
FDA UDI
Class IIActive
Ceramco 3 303530
FDA UDI
Class IIActive
Disposa-Shield® A88013
FDA UDI
Class IActive
Lucitone Digital IPN 3D Premium Tooth 906393
FDA UDI
Class IIActive
Sani-Tip® 122326N
FDA UDI
Class IActive
Ceramco 3 305206
FDA UDI
Class IIActive
Nupro® 801351
FDA UDI
Class IActive
Cavitron® 80393
FDA UDI
Class IIActive
Ceramco 3 303310
FDA UDI
Class IIActive
Cavitron® 80294
FDA UDI
Class IIActive
Ceramco 3 305016
FDA UDI
Class IIActive
Sani-Tip® 122212
FDA UDI
Class IActive
Disposa-Shield® 90736
FDA UDI
Class IActive
Ceramco 3 303880
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906387
FDA UDI
Class IIActive
Ceramco 3 305122
FDA UDI
Class IIActive
Ceramco 3 305119
FDA UDI
Class IIActive

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