We proudly announce that Silmet Ltd has been certified according to the EU Medical Device Regulation MDR 2017/745 . This latest certification means our complete product portfolio of Amalgams, Composites, Adhesives and Cements have now obtained EU MDR approval. Achieving EU MDR certification is a significant milestone for Silmet and marks our commitment to providing safe, effective, and cutting-edge dental restorative solutions.

Mr. Moshe Zalsman, CEO of Silmet stated that this certification demonstrates Silmet as being at the forefront of our commitment to ensuring that products adhere to the highest standards for the benefit of Silmet customers. We are one of the few companies in the dental restorative device field to achieve MDR certification for their products.

We are excited to share our latest collection of comprehensive case studies that demonstrate the exceptional performance and versatility of Silmet Dental restoration materials in real-world clinical settings.

These case studies provide in-depth insights into: Material performance under diverse dental restoration scenarios Successful patient outcomes Technical details of material usage

This Self-Adhesive Cement Kit is designed to meet the diverse needs of modern dental practices. It showcases a range of cement solutions, developed by Silmet and also includes a complementary modular drawer organizer to help the dentist keep their materials well-organized.

Each material has its own strengths and ideal applications:

Our brand-new catalog is out! The catalog offers an in-depth look at our entire range of dental restorative materials, including composites, bonding agents, sealers, and more. We’re introducing several new products that incorporate the latest advancements in dental material technology, providing you with high-performance solutions for all your restorative needs. Each product is clearly described with key features, benefits, High-quality images and application instructions to give you a better understanding of how our materials can improve your practice and help you choose the best materials.

The QMS has been appropriately updated to meet the requirements of MDR 2017/745. The company had documented a quality management system in accordance with the normative and regulatory requirements. The management system is based on the requirements of ISO 13485, EC Regulation 2017/475 and the country-specific requirements from Canada (SOR/98-282, Part 1) and USA (21 CFR Part 820 ff)

Dental cement is the most used material for dental practice to secure dental crowns, bridges, and orthodontic brackets in place. It can also be used to repair broken or chipped teeth.

Great Value Product! For the price of one branded product, try out 7 different products covering a very wide range of applications. ‍

ProLink Universal is a new addition to the ProLink line of adhesives.

Over the last 12 years, Silmet R&D gained knowledge and experience to overcome all challenges and develop ProLink Universal to perfection.

With less than a week to go until IDS 2023 opens its doors in Cologne, we look forward to joining the leading industry event and will be happy to meet you at IDS and use the chance to introduce our products and services.

We’ll be introducing a complimentary line of advanced dental luting and cementing materials. Enter our booth to learn about our New Product Launch and Silmet’s complete solution for dental restoration needs. Our exhibit team is ready to answer all your questions.

We are happy to announce that we were successfully audited for MDSAP:

The Medical Device Single Audit Program (MDSAP) is a program that allows the conduct of a single regulatory audit of a medical device manufacturer's quality management system to satisfy the requirements of multiple regulatory jurisdictions of up to five different medical device markets: Australia, Brazil, Canada, Japan and the United States. This certification is addition to being certified for ISO 13485:2016 and MDD.