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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 10 of 11
DeviceModel / ReferenceRegistriesClassStatus
Cavitron® 81510
FDA UDI
Class IIUnknown
Nupro® 965751
FDA UDI
Class IActive
Ceramco 3 305908
FDA UDI
Class IIActive
Ceramco 3 305101
FDA UDI
Class IIActive
Cavitron® 81503
FDA UDI
Class IIUnknown
Ceramco 3 303540
FDA UDI
Class IIActive
Nupro® 130315
FDA UDI
Class IIActive
Ceramco 3 305900
FDA UDI
Class IIActive
Ceramco 3 303050
FDA UDI
Class IIActive
Upgrade® 80953
FDA UDI
Class IActive
Cavitron® 8270310
FDA UDI
Class IIActive
Ceramco 3 305965
FDA UDI
Class IIActive
Cavitron® 81514
FDA UDI
Class IIUnknown
Sani-Tip® 122211
FDA UDI
Class IIActive
Ceramco 3 303440
FDA UDI
Class IIActive
Ceramco 3 303430
FDA UDI
Class IIActive
Cavitron® 8800301
FDA UDI
Class IIUnknown
Cavitron® 80293
FDA UDI
Class IIActive
Nupro® 130221
FDA UDI
Class IIActive
Ceramco 3 305121
FDA UDI
Class IIActive
Cavitron® 90146
FDA UDI
Class IActive
Ceramco 3 303840
FDA UDI
Class IIActive
Nupro® 130213
FDA UDI
Class IIActive
Delton® 27975
FDA UDI
Class IIActive
Nupro® 130323
FDA UDI
Class IIActive
Ceramco 3 305210
FDA UDI
Class IIActive
Ceramco 3 303220
FDA UDI
Class IIActive
Ceramco 3 305022
FDA UDI
Class IIActive
Cavitron® 8129503
FDA UDI
Class IIActive
Midwest® Rdh® 740050
FDA UDI
Class IActive
Nupro® 130314
FDA UDI
Class IIActive
Ceramco 3 303270
FDA UDI
Class IIActive
Cavitron® 82005
FDA UDI
Class IIActive
Nupro® 130083
FDA UDI
Class IActive
Cavitron® 81296
FDA UDI
Class IIUnknown
Cavitron® 82007
FDA UDI
Class IIActive
Cavitron® 8800402
FDA UDI
Class IIActive
Nupro® 130318
FDA UDI
Class IIActive
FASTips® 122505
FDA UDI
Class IActive
Ceramco 3 305139
FDA UDI
Class IIActive
Nupro® 130219
FDA UDI
Class IIActive
Nupro® 130226
FDA UDI
Class IIActive
Cavitron® 82001
FDA UDI
Class IIActive
Ceramco 3 305211
FDA UDI
Class IIActive
Ceramco 3 305114
FDA UDI
Class IIActive
Lucitone Digital IPN 3D Premium Tooth 906397
FDA UDI
Class IIActive
Nupro® 965213
FDA UDI
Class IActive
Nupro® 130211
FDA UDI
Class IIActive
Ceramco 3 305160
FDA UDI
Class IIActive
Cavitron® DualSelect™ 80529
FDA UDI
Class IActive

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