FGM Vittra APS Universal Dental Composite – 4g Syringe

FGM Vittra APS Universal Dental Composite – 4 g Syringe

FGM Vittra APS is a light-cured restorative dental composite for clinicians looking for a sculptable resin for anterior and posterior indications listed by the manufacturer. This listing covers one 4 g syringe in the selected shade.

Manufacturer information and clinical indications

FGM Vittra APS is a radiopaque, light-cured universal dental composite with spheroidal zirconium-silicate fillers and APS (Advanced Polymerization System) photoinitiator technology. FGM describes high polishability, a simplified shade system and a BPA-free formulation.

According to FGM, recommended uses include direct anterior and posterior restorations (Classes I–V), direct veneers, diastema closure, fragment bonding, core build-ups, selected repairs, and indirect inlays, onlays and veneers. Confirm the exact indication against the current instructions for use.

Handling and light curing

FGM recommends an incremental technique with increments up to 1.5 mm and the shade-specific light-curing exposure stated in the product instructions. Follow the adhesive manufacturer's instructions, use appropriate isolation, and confirm compatibility with the curing unit. Do not apply one universal curing time to all shades.

Choose your shade

Available Shopify shades: EA1, EA2, EA3, EB1, E Bleach, DA1, DA2, DA3 and DA3.5. Each selection has its own manufacturer SKU. Confirm the shade and SKU at checkout.

Frequently asked questions

Is Vittra APS used for posterior restorations?

FGM lists direct Class I–V restorations among the recommended indications, subject to its current IFU.

What comes in this listing?

One 4 g syringe in the chosen shade. Capsules are listed separately.

Explore dental composites and clinical guides

Browse FGM Vittra APS, FGM dental materials or our dental composite collection.

Manufacturer resource: FGM Vittra APS product information. Professional use only. Check the latest product-specific IFU and Canadian regulatory requirements before sale or clinical use.