Dentsply Palodent V3 Ring for Matrix Bands - Universal 2

The Dentsply Palodent V3 Ring, Universal 2, is an integral component of the Palodent V3 sectional matrix system, engineered to facilitate predictable and accurate contact creation in restorative dentistry. This system is specifically indicated for direct Class II composite restorations, encompassing conservative two-surface cavities, wider MOD preparations, and adjacent boxes. The Universal ring is designed to provide optimal separation and stability for matrix bands during these procedures, enhancing contact point formation crucial for successful restorative outcomes.

Constructed from nickel-titanium, the Palodent V3 Universal Ring offers outstanding spring strength and memory, ensuring consistent separation force. Its tines are made from glass-fiber reinforced plastic and are V-shaped to securely accommodate a wedge. This robust material composition contributes to the ring's durability and consistent performance.

The Palodent V3 Universal Ring is suitable for use with matrix bands in both direct and indirect restorations, particularly ideal for achieving optimal contact points in posterior restorations. The Universal rings are specifically designed for larger molars and can be stacked for versatility, allowing for simultaneous restoration of multiple surfaces. This system ensures accurate contacts and contours, even in challenging cases involving wide cavities and missing cusps.

Key Features : 

Designed for optimal separation and stability of matrix bands during restorative procedures, enhancing contact point formation.
Indicated for direct Class II composite restorations, including wider MOD preparations and adjacent boxes.
Features nickel-titanium construction for outstanding spring strength, memory, and consistent separation force.
Equipped with V-shaped, glass-fiber reinforced plastic tines to securely accommodate a wedge.
Suitable for larger molars and stackable for versatile use in simultaneous restoration of multiple surfaces.
Manufactured under a quality management system that complies with FDA 21 CFR Part 820 & 211 and ISO 13485:2003.
Conforms to the requirements of EU Directive 93/42/EEC, EU/2017/745, and UKMDR2002 for medical devices.