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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 3 of 11
DeviceModel / ReferenceRegistriesClassStatus
Delton® 27965
FDA UDI
Class IIActive
Nupro® 130212
FDA UDI
Class IIActive
Cavitron® 80399
FDA UDI
Class IIActive
FASTips® 122503
FDA UDI
Class IActive
Ceramco 3 303060
FDA UDI
Class IIActive
Sani-Tip® 122290N
FDA UDI
Class IActive
Delton® 310201
FDA UDI
Class IIActive
Cavitron® 130002
FDA UDI
Class IIActive
Cavitron® 79611
FDA UDI
Class IIActive
Cavitron® 82006
FDA UDI
Class IIActive
Cavitron® 7760201
FDA UDI
Class IIUnknown
Nupro® 965251
FDA UDI
Class IActive
Cavitron® 8800103
FDA UDI
Class IIActive
Cavitron® 79613
FDA UDI
Class IIActive
Ceramco 3 305961
FDA UDI
Class IIActive
Sani-Tip® 122320N
FDA UDI
Class IActive
Ceramco 3 303870
FDA UDI
Class IIActive
Nupro Freedom™ 90797
FDA UDI
Class IActive
Lucitone Digital IPN 3D Premium Tooth 906389
FDA UDI
Class IIActive
Ceramco 3 305118
FDA UDI
Class IIActive
Ceramco 3 303200
FDA UDI
Class IIActive
Ceramco 3 303350
FDA UDI
Class IIActive
Midwest® Rdh® 740030
FDA UDI
Class IActive
Cavitron® 8135204
FDA UDI
Class IIUnknown
Upgrade® 80954
FDA UDI
Class IActive
Ceramco 3 303400
FDA UDI
Class IIActive
Ceramco 3 305103
FDA UDI
Class IIActive
Ceramco 3 303590
FDA UDI
Class IIActive
Ceramco 3 303820
FDA UDI
Class IIActive
Delton® 2896
FDA UDI
Class IIActive
Ceramco 3 303520
FDA UDI
Class IIActive
Ceramco 3 305140
FDA UDI
Class IIActive
Midwest® 90702PK03
FDA UDI
Class IIUnknown
Midwest® Rdh® 740000
FDA UDI
Class IActive
Disposa-Shield® A88018
FDA UDI
Class IActive
Ceramco 3 303300
FDA UDI
Class IIActive
Ceramco 3 305223
FDA UDI
Class IIActive
Nupro® 130083
FDA UDI
Class IActive
Cavitron® 8135002
FDA UDI
Class IIUnknown
Ceramco 3 305130
FDA UDI
Class IIActive
Cavitron® 90148
FDA UDI
Class IActive
Ceramco 3 305903
FDA UDI
Class IIActive
Ceramco 3 305906
FDA UDI
Class IIActive
Ceramco 3 305230
FDA UDI
Class IIActive
Disposa-Shield® A880095
FDA UDI
Class IActive
Cavitron® 8135104
FDA UDI
Class IIUnknown
Ceramco 3 305173
FDA UDI
Class IIActive
Ceramco 3 305163
FDA UDI
Class IIActive
Cavitron® 8184002
FDA UDI
Class IIActive
Cavitron® 80398
FDA UDI
Class IIActive

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