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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 7 of 11
DeviceModel / ReferenceRegistriesClassStatus
Cavitron® 8800202
FDA UDI
Class IIActive
Ceramco 3 303710
FDA UDI
Class IIActive
Ceramco 3 305104
FDA UDI
Class IIActive
Sani-Tip® 120061
FDA UDI
Class IActive
Cavitron® 8135103
FDA UDI
Class IIUnknown
Cavitron® 80794
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906395
FDA UDI
Class IIActive
Cavitron® 80799
FDA UDI
Class IIActive
Ceramco 3 303730
FDA UDI
Class IIActive
Disposa-Shield® A88007
FDA UDI
Class IActive
Ceramco 3 305004
FDA UDI
Class IIActive
Ceramco 3 303150
FDA UDI
Class IIActive
Ceramco 3 303700
FDA UDI
Class IIActive
Cavitron® 8184001
FDA UDI
Class IIActive
Cavitron® 79362
FDA UDI
Class IIActive
Ceramco 3 305147
FDA UDI
Class IIActive
Ceramco 3 305137
FDA UDI
Class IIActive
Nupro® 130224
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906394
FDA UDI
Class IIActive
Midwest® Rdh® 740060
FDA UDI
Class IActive
Cavitron® 8800401
FDA UDI
Class IIActive
Ceramco 3 303850
FDA UDI
Class IIActive
Ceramco 3 305116
FDA UDI
Class IIActive
Nupro® 130317
FDA UDI
Class IIActive
Disposa-Shield® A88016
FDA UDI
Class IIActive
Ceramco 3 305015
FDA UDI
Class IIActive
Ceramco 3 303920
FDA UDI
Class IIActive
Ceramco 3 305146
FDA UDI
Class IIActive
Cavitron® 80394
FDA UDI
Class IIActive
Sani-Tip® 122336N
FDA UDI
Class IActive
Purevac® HVE 11020
FDA UDI
Class IActive
Nupro® 130327
FDA UDI
Class IIActive
Cavitron® 8129602
FDA UDI
Class IIUnknown
Cavitron® 8161425
FDA UDI
Class IIActive
Ceramco 3 303260
FDA UDI
Class IIActive
Ceramco 3 305136
FDA UDI
Class IIActive
Cavitron® 81502
FDA UDI
Class IIUnknown
Ceramco 3 305168
FDA UDI
Class IIActive
Sani-Tip® 122330N
FDA UDI
Class IActive
Ceramco 3 305911
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906398
FDA UDI
Class IIActive
Disposa-Shield® A88014
FDA UDI
Class IIActive
Ceramco 3 303420
FDA UDI
Class IIActive
Ceramco 3 303470
FDA UDI
Class IIActive
Cavitron® 81570
FDA UDI
Class IIActive
Ceramco 3 305149
FDA UDI
Class IIActive
Nupro® 130324
FDA UDI
Class IIActive
Ceramco 3 305403
FDA UDI
Class IIActive
Nupro® 130321
FDA UDI
Class IIActive
Cavitron® 8800007
FDA UDI
Class IIActive

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