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About us

Designed, developed, and produced in Lithuania, in compliance with European quality standards.

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Certificate_MDR 790107

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Certificate_ISO 13485

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Certificate_UKCA 790178

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Quality policy

Reliable solutions for everyday dentistry.

i-dental is a Lithuania-based manufacturer, distributor, importer of dental materials and system / pack producer. Our European quality standards ensure reliability, regulatory compliance, and clinically proven performance. For more than 30 years, we have been helping dentists find the best solutions for everyday practice.

The company was founded in 1994 as a dental materials supplier and in 2003 expanded into manufacturing, gaining full control over product quality and consistency. In 2020, we opened a new modern facility to work more efficiently, meet growing demand, and comply with the latest regulatory requirements.

Our commitment to quality

Quality at i-dental is defined by control, consistency, and compliance. Products are designed and manufactured in Lithuania, with every stage – formulation, production, filling, and packaging – completed in-house. This ensures full traceability and uniform quality across our portfolio.

Our certifications confirm compliance with the strictest European and international standards for design, manufacture and final inspection of non-sterile dental restorative and endodontic materials.

ISO 13485:2016

Quality Management System
Certificate No. MD 654577

Notified Body: BSI Group The Netherlands B.V.

Notified Body No: 2797

EU MDR (Regulation (EU) 2017/745)

EU Quality Management System
Certificate No. MDR 790107

Notified Body: BSI Group The Netherlands B.V.

Notified Body No: 2797

UK MDR 2002 (UKCA)

Full Quality Assurance System
Certificate No. UKCA 790178

Approved Body: BSI Assurance UK Ltd.

Approved Body No: 0086.

i-dental devices bear the CE 2797 and UKCA 0086 markings, issued by our Notified and Approved Bodies – one of the most respected conformity assessment bodies worldwide.

To ensure compliance with UK MDR 2002, i-dental has designated Premium Plus UK Limited (Bournemouth, UK) as its UK Responsible Person (UK REP), acting as the official point of contact with the MHRA.

For our partners and clinicians, this is more than regulatory compliance. It is a guarantee that every i-dental product is safe, reliable, and manufactured under the strictest quality supervision.

Summary of Safety and Clinical performance

When the European Database on Medical Devices comes online, the Summary of Safety and Clinical performance will be available at https://ec.europa.eu/tools/eudamed.

To request a copy of the Summary of Safety and Clinical Performance for UAB “Medicinos linija” medical devices, please send an email specifying the REF number(s) to info@i-dental.lt