The European medical device market is undergoing a critical transition. With the EU MDR, requirements for safety, clinical evaluation, documentation, and monitoring of medical devices are increasing. As a result, it is becoming increasingly important for users and partners to know which materials are already compliant with the new regulatory framework.

saremco print CROWNTEC meets the requirements of the MDR. For SAREMCO, this represents a significant regulatory milestone and, at the same time, an important step toward the long-term positioning of our 3D printing material in the European dental market. Innovation and regulatory certainty thus go hand in hand.

saremco print CROWNTEC was developed for the additive manufacturing of dental restorations. The range of indications includes permanent crowns, inlays, onlays, veneers, and prosthetic teeth, as well as specific temporary restorations. With a flexural strength of over 135 MPa, CROWNTEC combines mechanical performance with the aesthetic requirements of modern digital dentistry.