INTERDENT proizvodnja in trgovina, d.o.o.

INTERDENT produces dental materials primarily used for temporary restorations and preparations. Their portfolio includes polymethyl methacrylate (PMMA) composite disks, zirconia-based composite disks (including multilayer variants), cold-curing acrylic resin (INTERACRYL COLD), and wooden interdental wedges. These devices are designed for crown and bridge procedures, as well as dental spacing applications.

The company is based in Slovenia, as indicated by its country designation (SI). This geographical location is relevant for regulatory compliance and device classification under EU Medical Device Regulations.

INTERDENT’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registration is required for compliance with the EU Medical Device Regulations (MDR) and ensures traceability of devices under the EU’s regulatory framework.

INTERDENT’s devices fall under Class I or Class IIa classifications according to the EU Medical Device Regulations. Classification depends on factors like intended use, risk level, and duration of contact with the patient. For example, temporary restorative materials like PMMA disks and zirconia composites are typically Class IIa due to their role in dental procedures, while lower-risk items like wooden wedges may qualify as Class I.