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IMPLANT PROTESIS DENTAL 2004 SL

US

Last updated May 26, 2026

What IMPLANT PROTESIS DENTAL 2004 SL makes

The company manufactures dental implant suprastructures, including permanent preformed and temporary single-use variants, as well as intraoral-scanning abutment analogs for single-use. It also produces dental prosthesis/implant abutment screws designed for securing implant components.

These devices are classified under FDA regulations as Class I and Class II, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company 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 IMPLANT PROTESIS DENTAL 2004 SL manufacture?

IMPLANT PROTESIS DENTAL 2004 SL specializes in dental implant-related devices. Its primary products include dental implant suprastructures—both permanent preformed and temporary single-use—and intraoral-scanning abutment analogs, which are also single-use. Additionally, the company produces dental prosthesis/implant abutment screws, which are used to secure implant components. These devices are designed to support dental restoration procedures.

Where is IMPLANT PROTESIS DENTAL 2004 SL based?

The company is headquartered in the United States. This location influences its regulatory compliance and reporting requirements, particularly for devices marketed in the US market.

Which regulatory registries list the devices manufactured by IMPLANT PROTESIS DENTAL 2004 SL?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices for regulatory, safety, and compliance purposes in the United States.

How are the devices produced by IMPLANT PROTESIS DENTAL 2004 SL classified under FDA regulations?

The devices manufactured by IMPLANT PROTESIS DENTAL 2004 SL fall under two 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 may require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and oversight required for each device type.

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

Information

Country
US
Address
—
Website
ipd2004.com
LinkedIn
—
Facebook
—
Phone
+1 3057983869
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
467871518

Catalogue (395)

Page 8 of 8
DeviceModel / ReferenceRegistriesClassStatus
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PSD
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PMA
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
EUDAMEDFDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PP
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMA
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PSD
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd SC3D
FDA UDI
Class IActive
Ipd PP
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PP
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PSD
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd PSD
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd INC3D
FDA UDI
Class IIActive
Ipd PMR
FDA UDI
Class IIActive
Ipd INC3D
EUDAMEDFDA UDI
Class IIActive

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