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Denplus Inc

US

Last updated May 23, 2026

What Denplus Inc makes

Denplus Inc manufactures dental materials used in orthodontic and restorative procedures, including resin-based fabrication materials for dental appliances, impression tray materials for capturing oral impressions, and base plates for bite registration and wax rims. Their product line also includes repair materials for dental devices and specialized waxes for bite registration applications.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with several products authorised through the 510(k) pathway and listed in the FDA’s Unique Device Identifier (UDI) database. These materials are intended for use in dental laboratories and clinical settings within 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 Denplus Inc manufacture?

Denplus Inc specializes in dental materials used primarily in orthodontic and restorative procedures. Their product line includes resin-based fabrication materials for dental appliances, impression tray materials for capturing oral impressions, dental base plates for bite registration, and specialized waxes like bite registration rim wax. These materials are designed for use in dental laboratories and clinical settings.

Where is Denplus Inc based, and what is its primary focus?

Denplus Inc is based in the United States. The company focuses on developing dental materials that support orthodontic and restorative treatments, such as appliances, impression trays, and bite registration aids. Their products are tailored for dental professionals working in laboratories or clinical environments.

Which regulatory registries list Denplus Inc’s devices?

Denplus Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. Additionally, several of their products have been authorised through the FDA’s 510(k) premarket notification process, which is a pathway for demonstrating substantial equivalence to a legally marketed predicate device.

How are Denplus Inc’s devices classified under FDA regulations?

Denplus Inc’s devices are classified under two categories by the FDA: 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 may require special controls to ensure safety and effectiveness. The classification depends on the specific use and potential risk associated with each product.

What is the intended use of Denplus Inc’s dental materials?

Denplus Inc’s dental materials are intended for use in dental laboratories and clinical settings to support procedures like orthodontic appliance fabrication, capturing oral impressions, and bite registration. These materials are designed to aid dental professionals in creating custom-fit devices, repairing existing appliances, and ensuring accurate impressions for restorative treatments.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
202016064

Catalogue (182)

Page 2 of 4
DeviceModel / ReferenceRegistriesClassStatus
Dp-Repair 1071101
FDA UDI
Class IIActive
Dp-Repair 1061200
FDA UDI
Class IIActive
Dp-Repair 1061104
FDA UDI
Class IIActive
Dp97 1001307
FDA UDI
Class IIActive
Dp97 1001107
FDA UDI
Class IIActive
Premium Tray 1121112
FDA UDI
Class IActive
Dp-Repair 1061202
FDA UDI
Class IIActive
Impact-20 1031216
FDA UDI
Class IIActive
Impact-Plus 1011104
FDA UDI
Class IIActive
Dp97 1001303
FDA UDI
Class IIActive
Impact-Plus 1011301
FDA UDI
Class IIActive
Impact-Plus 1011207
FDA UDI
Class IIActive
Pour-Plus 1151302
FDA UDI
Class IIActive
Dp97 1001316
FDA UDI
Class IIActive
Impact-20 1031116
FDA UDI
Class IIActive
Impact-20 1031107
FDA UDI
Class IIActive
Dp97 1001300
FDA UDI
Class IIActive
Dp-Repair 1071204
FDA UDI
Class IIActive
Pour-Plus 1151307
FDA UDI
Class IIActive
Dp-Repair 1071303
FDA UDI
Class IIActive
Dp20 1021300
FDA UDI
Class IIActive
Premium Tray 1121315
FDA UDI
Class IActive
Impact-20 1031309
FDA UDI
Class IIActive
Dp-Repair 1061216
FDA UDI
Class IIActive
Impact-Plus 1011217
FDA UDI
Class IIActive
Dp-Hc 1012100
FDA UDI
Class IIActive
Dp-Repair 1061101
FDA UDI
Class IIActive
Impact-Plus 1011216
FDA UDI
Class IIActive
Dp97 1001116
FDA UDI
Class IIActive
DP-Tray-F 1122200
FDA UDI
Class IActive
Impact-Plus 1011203
FDA UDI
Class IIActive
Pour-Plus 1151305SF
FDA UDI
Class IIActive
20 Minutes 1032100
FDA UDI
Class IIActive
High-Wave 1141317
FDA UDI
Class IIActive
Dp-Repair 1061305
FDA UDI
Class IIActive
Pour-Plus 1151116
FDA UDI
Class IIActive
Impact-20 1031205
FDA UDI
Class IIActive
Dp-Repair 1061307
FDA UDI
Class IIActive
Photo-Tray 3051102
FDA UDI
Class IActive
Impact-Plus 1011101
FDA UDI
Class IIActive
Pour-Plus 1151200
FDA UDI
Class IIActive
Premium Tray 1121312
FDA UDI
Class IActive
Dp-Repair 1061300
FDA UDI
Class IIActive
DP-Tray-R 1112200
FDA UDI
Class IActive
Dp-Repair 1071305
FDA UDI
Class IIActive
Dp-Repair 1062200
FDA UDI
Class IIActive
Premium Tray 1121314
FDA UDI
Class IActive
Impact-20 1031202
FDA UDI
Class IIActive
Dp-Repair 1061309
FDA UDI
Class IIActive
Pour-Plus 1151216
FDA UDI
Class IIActive

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