OMNICHROMA BLOCKER

Ideal supplement for Omnichroma when it comes to extensive Class III and Class IV restorations or for masking discolourations
OMNICHROMA BLOCKER single syringe
Article code: 10113

The ideal supplement for OMNICHROMA!

OMNICHROMA BLOCKER is used if OMNICHROMA is not to adjust to the colour of a strongly discoloured cavity or if a higher opacity is required to cover the oral cavity in the case of larger class III or IV defects.

The general recommendation for the use of OMNICHROMA BLOCKER is an incremental thickness of 0.5 mm. In the case of very opaque anterior teeth or strong discolourations, however, a larger layer thickness may also be necessary.

Indications

✔ Masking of slight discolourations
✔ Reconstructing highly opaque tooth

Available colours

✔ Opaque

Properties and benefits

✔ Ideal supplement for OMNICHROMA
✔ Good polishability
✔ Masking effect

Blocker in clinical use

The general recommendation for the use of OMNICHROMA BLOCKER is a incremental thickness of 0.5mm. In the case of very opaque anterior teeth or strong discolourations, however, a larger layer thickness may also be necessary.

omnichroma-blocker-cavityLeft: Discoloured cavity floor // Right: OMNICHROMA BLOCKER (Tokuyama Dental)

Packaging

✔ Refill: 1 single syringe (4g)
✔ Refill: 20 capsules (0.2g each)

These dentists recommend this product

My first reaction was that OMNICHROMA is truly magic. The result is also beutiful, high gloss, easy to sculpt and the procedure is simple. Except for the fact that you can skip the shade selection step your workflow is the same as with regular composites. The only addition is the blocker which you can use to cover heavy discolouration which you don´t want the composite to take it´s colour from.

Dr. Clas Oscarsson

"The use of the blocker requires a little bit of intuition, but even anterior restorations can be solved excellently with OMNICHROMA."

Dr. Christof Föcking

Awarded products - multiple certified service

  • * Our Class IIa devices are certified as a medical device in the European Union under the Medical Device Directive 93/42/EEC by SGS CE1639, exclusively for the indication(s) detailed into the corresponding IFUs. Other non-medical uses ascribed to these devices are not within the scope of CE certification, and users should be aware product performance and/or safety has not been evaluated by SGS for those purposes.