Ivoclar Vivadent Tetric N-Ceram Bulk Fill Syringe Refills Packable Composite Resin - IVW

Ivoclar Vivadent Tetric N-Ceram Bulk Fill Syringe Refills are a light-curing, packable composite resin engineered for efficient direct restorations. This nano-optimized hybrid composite is formulated for simplified and time-saving application across various dental procedures.

Utilizing advanced bulk fill technology, Tetric N-Ceram Bulk Fill allows for the placement of material in increments up to 4 mm in a single layer, thereby streamlining the restorative process. Its composition includes a methacrylate-based matrix and specialized inorganic fillers, alongside the patented Ivocerin light initiator, which ensures reliable polymerization even in deeper cavities.

This composite resin is indicated for direct restorations in posterior teeth (Classes I and II), Class V restorations (cervical caries, root erosions, wedge-shaped defects), restoration of deciduous teeth, extended fissure sealing in molars and premolars, and reconstructive build-ups. A specially conditioned shrinkage stress reliever is incorporated to minimize polymerization shrinkage and stress, contributing to the longevity and stability of the restoration.

Key Features : 

A light-cured, hybrid composite suitable for direct restorations in posterior teeth (Classes I and II), Class V restorations, extended fissure sealing in molars and premolars, reconstructive build-ups, and restoration of deciduous teeth.
Designed for bulk placement in increments of up to 4 mm, reducing the need for multiple layers and optimizing procedural time.
Provides a working time of more than three minutes under defined light conditions of 8000 lux, allowing for ample time for contouring.
Achieves a short curing time of 10 seconds when exposed to a light intensity of ≥ 1,000 mW/cm², utilizing blue light in the 400–500 nm wavelength range for efficient polymerization.
Incorporates a shrinkage stress reliever to minimize volumetric shrinkage and stress during polymerization, enhancing marginal integrity and restoration durability.
Classified as a medical device in accordance with Directive 93/42/EEC.