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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 6 of 11
DeviceModel / ReferenceRegistriesClassStatus
Ceramco 3 305220
FDA UDI
Class IIActive
Delton® 2695
FDA UDI
Class IIActive
Ceramco 3 305915
FDA UDI
Class IIActive
Ceramco 3 303890
FDA UDI
Class IIActive
Nupro® 130215
FDA UDI
Class IIActive
Ceramco 3 305960
FDA UDI
Class IIActive
Ceramco 3 305910
FDA UDI
Class IIActive
Ceramco 3 305007
FDA UDI
Class IIActive
Ceramco 3 305021
FDA UDI
Class IIActive
Cavitron® 80400
FDA UDI
Class IIActive
Cavitron® 8800502
FDA UDI
Class IIActive
Ceramco 3 305145
FDA UDI
Class IIActive
Cavitron® 8800002
FDA UDI
Class IIActive
Nupro® 965768
FDA UDI
Class IActive
Ceramco 3 305102
FDA UDI
Class IIActive
Ceramco 3 303320
FDA UDI
Class IIActive
Cavitron® 8195001
FDA UDI
Class IIActive
Midwest® Rdh® 740010
FDA UDI
Class IActive
Nupro® 965259
FDA UDI
Class IActive
Cavitron® 90260
FDA UDI
Class IIActive
Nupro® 965253
FDA UDI
Class IActive
Ceramco 3 305167
FDA UDI
Class IIActive
Ceramco 3 305164
FDA UDI
Class IIActive
Cavitron® 8270313
FDA UDI
Class IIActive
Ceramco 3 303490
FDA UDI
Class IIActive
Ceramco 3 303780
FDA UDI
Class IIActive
Cavitron® 8800203
FDA UDI
Class IIActive
Ceramco 3 305019
FDA UDI
Class IIActive
Cavitron® 8135203
FDA UDI
Class IIUnknown
Ceramco 3 305131
FDA UDI
Class IIActive
Cavitron® 8250001
FDA UDI
Class IIUnknown
Ceramco 3 305006
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906383
FDA UDI
Class IIActive
Ceramco 3 303640
FDA UDI
Class IIActive
Ceramco 3 303630
FDA UDI
Class IIActive
Nupro® 130322
FDA UDI
Class IIActive
Ceramco 3 305141
FDA UDI
Class IIActive
Ceramco 3 305202
FDA UDI
Class IIActive
Ceramco 3 303770
FDA UDI
Class IIActive
Nupro Freedom™ 90799
FDA UDI
Class IActive
Nupro® 965256
FDA UDI
Class IActive
Nupro® 965755
FDA UDI
Class IActive
Ceramco 3 303790
FDA UDI
Class IIActive
Nupro® 965254
FDA UDI
Class IActive
Cavitron® 63740
FDA UDI
Class IIActive
Ceramco 3 303330
FDA UDI
Class IIActive
Nupro® 130210
FDA UDI
Class IIActive
Purevac® HVE 11000
FDA UDI
Class IActive
Cavitron® 8270311
FDA UDI
Class IIActive
Seal & Protect™ 658010
FDA UDI
Class IIActive

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