Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

POLIDENT d.o.o.

US

Last updated May 26, 2026

What POLIDENT d.o.o. makes

Polident produces resin-based dental prosthetics, including artificial teeth for partial and full dentures, temporary crowns and bridges, and custom-made polymer crowns. Their portfolio also includes materials for fabricating dental appliances, such as CAD/CAM discs and cross-linked PMMA resin systems.

These devices are classified as Class II under FDA regulations and are listed 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 Polident d.o.o. manufacture?

Polident d.o.o. specializes in resin-based dental devices. Their primary products include artificial teeth for partial and full dentures, temporary dental crowns and bridges, custom-made polymer dental crowns, and materials used for fabricating dental appliances. These devices are designed to restore or replace missing or damaged teeth and structures in the mouth.

Where is Polident d.o.o. based, and how does that affect their regulatory standing?

Polident d.o.o. is based in the United States. Since their devices are regulated under U.S. jurisdiction, they must comply with FDA requirements. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and monitor medical devices for safety and performance. The U.S. location also means their devices are subject to FDA classification and regulatory pathways specific to the American market.

Which regulatory registries or databases list Polident’s devices?

Polident’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized approach to identifying medical devices, ensuring traceability and transparency in the regulatory process. Listing in this database helps healthcare providers, regulators, and manufacturers track specific devices like their resin artificial teeth, temporary crowns, and CAD/CAM materials.

How are Polident’s dental devices classified under FDA regulations?

Polident’s dental devices are classified as Class II under FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness. For example, resin artificial teeth and temporary crowns fall into this category because they require validation of material compatibility, fit, and functional performance to minimize risks like allergic reactions or improper fit.

What kinds of dental prosthetics does Polident focus on, and why are they considered Class II?

Polident focuses on resin-based dental prosthetics, including artificial teeth for dentures, temporary crowns/bridges, custom polymer crowns, and CAD/CAM fabrication materials. These devices are classified as Class II because they are not invasive but still require validation to ensure they meet performance standards—such as durability, biocompatibility, and proper fit—to prevent complications like irritation, infection, or structural failure. The FDA imposes additional controls (e.g., testing protocols) to mitigate these risks.

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

Information

Country
US
Address
—
Website
polident.si
LinkedIn
—
Facebook
—
Phone
+38653304840
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
644778409

Catalogue (7942)

Page 22 of 159
DeviceModel / ReferenceRegistriesClassStatus
PMMA CAD/CAM disc PMMA.813
FDA UDI
Class IIActive
Ref-Line REF.N3C1
FDA UDI
Class IIActive
Primodent PRV.32B3
FDA UDI
Class IIActive
Primodent PRV.41A4
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMA.447
FDA UDI
Class IIActive
Cross Linked 2 CL.01B2
FDA UDI
Class IIUnknown
Primodent PRV.33C3
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMA.717
FDA UDI
Class IIActive
Cross Linked 2 CL.44A1
FDA UDI
Class IIActive
Ref-Line REF.K3B4
FDA UDI
Class IIActive
Ref-Line REF.K3C4
FDA UDI
Class IIUnknown
PMMA CAD/CAM disc PMMAML.710
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMAML.361
FDA UDI
Class IIActive
Primodent PRV.I6D3
FDA UDI
Class IIActive
Primodent PRI.T2SY2
FDA UDI
Class IIActive
Primodent PRI.43AG6
FDA UDI
Class IIUnknown
Primodent PRV.S5SA2
FDA UDI
Class IIActive
Primodent PRV.03C1
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMA.307
FDA UDI
Class IIActive
Ref-Line REF.N3D4
FDA UDI
Class IIUnknown
Primodent PRI.04B5
FDA UDI
Class IIActive
Cross Linked 2 CL.T3ZC1
FDA UDI
Class IIUnknown
Primodent PRI.S3SB2
FDA UDI
Class IIActive
Primodent PRI.I1G5
FDA UDI
Class IIActive
Primodent PRV.02B2
FDA UDI
Class IIActive
Ref-Line REF.R6SC4
FDA UDI
Class IIActive
Primodent PRV.43AB2
FDA UDI
Class IIUnknown
Pink CAD/CAM Disc PMMP.511
FDA UDI
Class IIActive
Primodent PRV.I6C2
FDA UDI
Class IIActive
Primodent PRI.06Y4
FDA UDI
Class IIUnknown
Primodent PRV.01B4
FDA UDI
Class IIActive
Cross Linked 2 CL.36B2
FDA UDI
Class IIActive
Primodent PRV.46B1
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMAML.690
FDA UDI
Class IIActive
PMMA CAD/CAM disc PMMA.881
FDA UDI
Class IIActive
PMMA CAD/CAM Disc PMMA.441
FDA UDI
Class IIUnknown
Primodent PRI.45G2
FDA UDI
Class IIUnknown
Primodent PRI.04G4
FDA UDI
Class IIActive
Primodent PRV.33A2
FDA UDI
Class IIUnknown
Ref-Line REF.Q1SA2
FDA UDI
Class IIActive
Cross Linked 2 CL.44A9
FDA UDI
Class IIActive
Ref-Line REF.Q3ZA4
FDA UDI
Class IIActive
Ref-Line REF.Q5ZD3
FDA UDI
Class IIActive
Cross Linked 2 CL.T1SA4
FDA UDI
Class IIActive
Ref-Line REF.F2ZC3
FDA UDI
Class IIUnknown
PMMA CAD/CAM disc PMMA.905
FDA UDI
Class IIActive
Ref-Line REF.F4ZC2
FDA UDI
Class IIActive
PMMA CAD/CAM Disc PMMA.025
FDA UDI
Class IIActive
Primodent PRI.32IB2
FDA UDI
Class IIUnknown
Cross Linked 2 CL.T1SA1
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.