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 39 of 159
DeviceModel / ReferenceRegistriesClassStatus
Primodent PRV.44D4
FDA UDI
Class IIUnknown
Primodent PRI.03G6
FDA UDI
Class IIUnknown
Cross Linked 2 CL.44A4
FDA UDI
Class IIUnknown
Primodent PRI.44Y6
FDA UDI
Class IIUnknown
Primodent PRI.I6Y4
FDA UDI
Class IIUnknown
Primodent PRV.T4SA1
FDA UDI
Class IIActive
Primodent PRV.T4SA4
FDA UDI
Class IIUnknown
PMMA CAD/CAM Disc PMMA.169
FDA UDI
Class IIActive
Cross Linked 2 CL.36C4
FDA UDI
Class IIActive
Primodent PRI.T3SG6
FDA UDI
Class IIActive
Primodent PRI.T4SB1
FDA UDI
Class IIUnknown
Ref-Line REF.M6D3
FDA UDI
Class IIUnknown
Primodent PRV.04A3
FDA UDI
Class IIActive
Cross Linked 2 CL.T5ZA1
FDA UDI
Class IIUnknown
Primodent PRI.S5SG4
FDA UDI
Class IIActive
Ref-Line REF.R2ZC2
FDA UDI
Class IIActive
Primodent PRV.32ID2
FDA UDI
Class IIActive
Primodent PRV.31B3
FDA UDI
Class IIUnknown
Primodent PRV.T1ZA2
FDA UDI
Class IIUnknown
Ref-Line REF.U3A9
FDA UDI
Class IIActive
Primodent PRI.43AB3
FDA UDI
Class IIUnknown
PMMA CAD/CAM disc PMMA.243
FDA UDI
Class IIActive
Primodent PRI.I6G5
FDA UDI
Class IIUnknown
Ref-Line REF.R2ZB1
FDA UDI
Class IIUnknown
Primodent PRI.I7G2
FDA UDI
Class IIUnknown
Cross Linked 2 CL.35L3
FDA UDI
Class IIUnknown
Cross Linked 2 CL.45C4
FDA UDI
Class IIActive
Cross Linked 2 CL.36D3
FDA UDI
Class IIActive
Primodent PRV.S3SC1
FDA UDI
Class IIUnknown
Primodent PRV.32IA2
FDA UDI
Class IIActive
Primodent PRI.31B3
FDA UDI
Class IIActive
Ref-Line REF.Q3ZB4
FDA UDI
Class IIActive
Ref-Line REF.F2SC1
FDA UDI
Class IIUnknown
Primodent PRV.T6ZB4
FDA UDI
Class IIActive
Primodent PRV.S1SD4
FDA UDI
Class IIUnknown
Primodent PRI.L6G2
FDA UDI
Class IIUnknown
Primodent PRI.I4B5
FDA UDI
Class IIActive
PMMA CAD/CAM Disc PMMA.698
FDA UDI
Class IIUnknown
Ref-Line REF.M6A1
FDA UDI
Class IIUnknown
Ref-Line REF.R4SA4
FDA UDI
Class IIUnknown
Primodent PRI.L2B3
FDA UDI
Class IIUnknown
Ref-Line REF.R6SC1
FDA UDI
Class IIActive
Primodent PRI.37AY0
FDA UDI
Class IIActive
Primodent PRI.03Y2
FDA UDI
Class IIUnknown
Ref-Line REF.M4L3
FDA UDI
Class IIUnknown
Ref-Line REF.H6C3
FDA UDI
Class IIActive
Primodent PRV.I3B3
FDA UDI
Class IIActive
Primodent PRV.I2D2
FDA UDI
Class IIActive
Primodent PRI.T1ZB2
FDA UDI
Class IIUnknown
Ref-Line REF.N6D3
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.