Yes. Biodentine® XP is a suitable dental material for primary (children 2+) and permanent teeth in accordance with its IFU. Biodentine® XP is favored in vital pulp therapy in young patients due to its excellent safety profile, biocompatibility, and bioactivity*****. Biodentine® XP’s benefits include:
• Preserving pulp vitality in deep caries or accidental pulp exposure.
• Promoting dentine bridge formation to protect the natural tooth structure.
• Supporting continued root development in immature permanent teeth by maintaining the health of the radicular pulp.
Biodentine® XP can be used in pediatric dentistry as a bulk-filling material. Using the Bio-Bulk Fill procedure*, the final restoration can be placed in the same visit.
***** Properties verified by preclinical studies.
Biodentine® XP cartridges have a shelf life of 24 months from the date of manufacture when storage recommendations are followed. To ensure product longevity:
Discard any Biodentine® XP cartridges that have exceeded the expiry date on the packaging.
Biodentine® is a dentine substitute with multiple clinical applications.
In the crown, it can be used for temporary dentine-enamel restoration for up to 6 months, restoration of deep and/or large coronal carious lesions, restoration of cervical or radicular lesions, pulp capping (direct and indirect), and pulpotomy for diagnosed symptoms of reversible or irreversible pulpitis.
Biodentine®’s unique combination of therapeutic and restorative properties makes it optimal for filling the tooth from pulp to crown using the Bio Bulk-Fill procedure. As only one material is used, it’s not necessary to use layering and light curing. The final enamel restoration can be placed in the same session, offering greater time-efficiency for practitioners, and fewer visits and less chair time for patients.
Biodentine® is a unique combination of pulp therapeutic and restorative properties in one material, ideal for daily deep cavities restorations with the Bio-Bulk Fill procedures. Some of the materials commonly used for similar indications include:
In conclusion, while there are a number of restorative materials on the market, numerous clinical and preclinical studies have reported favorable outcomes with Biodentine® in terms of handling, setting, sealing8, biocompatibility9, and bioactivity7, 10.
Biodentine® XP is a dentine restoration system designed for daily deep cavity restorations. It represents the next generation of Biodentine®, a unique material combining both therapeutic and restorative properties.
Biodentine® XP is made from ultra-pure tricalcium silicate using proprietary Active Biosilicate (ABS) Technology™, providing biocompatibility and bioactivity. Suitable for indirect or direct placement over the pulp, Biodentine® XP stimulates the pulp’s healing capabilities and promotes the formation of reparative dentine to help maintain tooth vitality and structure.
Biodentine® XP forms an interface with the dentine surface via micromechanical anchorage, providing a tight seal. Thanks to its long-lasting dimensional stability, Biodentine® maintains this seal over time and resists microleakage. It reaches mechanical properties similar to sound dentine, making it an optimal choice for bulk-filling techniques such as the Bio-Bulk Fill procedure.
Biodentine® is a unique combination of pulp therapeutic and restorative properties in one material, ideal for daily deep cavities restorations with the Bio-Bulk Fill procedures. Some of the materials commonly used for similar indications include:
In conclusion, while there are a number of restorative materials on the market, numerous clinical and preclinical studies have reported favorable outcomes with Biodentine® in terms of handling, setting, sealing8, biocompatibility9, and bioactivity3, 10.
The Biodentine® powder component comes in a capsule and is composed of:
The Biodentine® liquid component comes in an ampoule and contains:
Biodentine® has an initial setting time of approximately 12 minutes after mixing. It is recommended to wait 12-15 minutes before covering with the final restoration in order for Biodentine® to fully set.
The setting time may vary (from 9 to 25 minutes) depending on certain conditions, including the storage time and storage conditions.
Biodentine® and Biodentine® XP are both made from the same materials: ultra-pure tricalcium silicate powder, calcium carbonate, zirconium oxide, and a calcium chloride liquid with a water-soluble polymer. Therefore, there is no difference in composition, clinical applications, or benefits.
The key difference between Biodentine® and Biodentine® XP is the method of preparation and delivery. Biodentine® capsules contain the powder component, which must be mixed with the calcium chloride solution using a triturator/amalgamator machine. It creates a paste-like material that is then placed in the tooth with an applicator tool, e.g. spatula. Biodentine® XP comes in a syringe-like cartridge that contains both the Biodentine® liquid and powder components in one. The cartridge is placed in the high-speed Biodentine® XP Mixer to combine the ingredients into a smooth, flowable paste, which is then placed directly into the tooth using the Biodentine® XP Dispenser Gun for crown indications.
Alternatively, you may apply Biodentine® XP with an amalgam carrier, a spatula, or a Root Canal Messing Gun.
Although there is no difference in terms of clinical efficacy, certain applications are generally better suited to one system over the other. Specifically, Biodentine® XP simplifies daily deep cavities restorations with direct placement in the tooth thanks to the Biodentine® XP Dispenser Gun and Biodentine® XP cartridge format.
Biodentine® is a dentine substitute with multiple clinical applications. In the crown, it can be used for temporary dentine-enamel restoration for up to 6 months, restoration of deep and/or large coronal carious lesions, restoration of cervical or radicular lesions, pulp capping (direct and indirect), and pulpotomy for diagnosed symptoms of reversible or irreversible pulpitis. In the root, Biodentine® can be used for root and furcation perforations, internal/external resorptions, apexification, retrograde surgical filling, and revitalization.
Biodentine®’s unique combination of therapeutic and restorative properties makes it adequate for filling the tooth from pulp to crown using the Bio Bulk-Fill procedure. As only one material is used, it’s not necessary to use layering and light curing. The final enamel restoration can be placed in the same session, offering greater time-efficiency for practitioners, and fewer visits and less chair time for patients.
* Properties verified by preclinical studies
Biodentine® is a dentine restoration material that acts as both a pulp therapeutic and restorative material for daily deep cavity restorations. It is made from ultra-pure tricalcium silicate using proprietary Active Biosilicate (ABS) Technology™, offering exceptional biocompatibility and bioactivity*. made from ultra-pure tricalcium silicate using proprietary Active Biosilicate (ABS) Technology™, offering exceptional biocompatibility and bioactivity.
Suitable for indirect or direct placement over the pulp, Biodentine® stimulates the pulp’s healing capabilities and promotes the formation of reparative dentine to help maintain tooth vitality and structure. Biodentine® forms an interface with the dentine surface via micromechanical anchorage, providing a tight seal. Thanks to its long-lasting dimensional stability, Biodentine® maintains this seal over time and resists microleakage. It reaches mechanical properties similar to sound dentine, making it an adequate choice for bulk-filling techniques such as the Bio-Bulk Fill procedure.
* Properties verified by preclinical studies
OraSoothe Rinse (Professional and Hygiene) is an oral coating rinse. It is noticeably thicker than mouthwash and is designed to coat the mouth. OraSoothe contains all-natural ingredients and is designed to be swallowed if desired. OraSoothe provides fast pain relief without numbing the mouth. OraSoothe Rinse is also shown to inhibit microbial contamination Orasoothe provides an optimal oral wound healing environment.
First, swishing the rinse creates an ultra-thin film that protects the mouth from further irritation and contamination. Second, the negatively-charged gel binds the positively-charged sodium. This prevents the pain signal from being transmitted to the brain.
OraSoothe does not numb the mouth like topical anesthetics (benzocaine, lidocaine, etc.) Unlike these drugs, OraSoothe is not absorbed into tissues and does not alter cell physiology.
OraSoothe Professional Rinse and OraSoothe Hygiene Rinse are made from food ingredients, with no artificial components. They contain mannose polysaccharides from Aloe vera, xylitol and a tiny amount of essential oils of cinnamon, clove, thyme, and wintergreen.
Companies that have reimbursed for treatment with OraSoothe include Aetna, United Healthcare, Cigna, Delta Dental, Comp Dent, Met Life, and others. Insurance code 9630 is used.
Enough OraSoothe Gel should be applied to the extraction site to completely coat and cover the wound. Excess gel will not remain in place and will be swallowed.
OraSoothe ‘Sockit’ Gel is made from food ingredients, with no artificial components. OraSoothe contains mannose polysaccharides from Aloe vera, xylitol and a tiny amount of essential oils of cinnamon, clove, and thyme.
Yes R.T.R.+ is fully resorbable.
Both B-TCP and Hydroxyapatite are 100% resorbable but on different pace. The benefits of R.T.R.+ particularly come from this appropriate balance between both components:
– The fast acting B-TCP
– The slower resorption Hydroxyapatite that provide the right scaffold and hence the high stability
Therefore the resorption time can be adapted to the clinical situation.
The range allows you to choose the pace of your bone graft procedure
– If you require a socket filling with a fast new bone formation to prevent future bone weakness, R.T.R.+ 80/20 might be your preferred choice.
– If you prefer a longer resorption pace, hence an even more stable new bone formation, then R.T.R.+ 40/60 will certainly be your choice
Obviously, both treatments are of a high quality and allow future implant placement.
Yes, R.T.R.+ is fully synthetic, which offers a high success rate with no risk associated.
The R.T.R. Membrane can be placed either dry or hydrated. If the clinician prefers the handling characteristics of the hydrated collagen, the membrane can be hydrated in sterile water or saline solution prior to final placement.
Yes, R.T.R. Membrane is compatible with R.T.R.+
R.T.R. Membrane exists in 2 sizes to meet clinical needs:
– 15 x 20mm
– 20 x 30mm
Yes, R.T.R. Membrane is fully resorbable in 4 to 8 weeks.
None of the ingredients of our product Septocaine® and epinephrine 1:200,000 are an evident source of peanut, soy or nut.
None of the ingredients of our product Septocaine® and epinephrine 1:200,000 are an evident source of alcohol.
None of the ingredients of our product Septocaine® and epinephrine 1:200,000 are an evident source of gluten.
None of the ingredients of our product Septocaine® and epinephrine 1:100,000 are an evident source of peanut, soy or nut.
None of the ingredients of our product Septocaine® and epinephrine 1:100,000 are an evident source of alcohol.
None of the ingredients of our product Septocaine® and epinephrine 1:100,000 are an evident source of gluten.
None of the ingredients of our product Scandonest® 3% plain are an evident source of peanut, soy or nut.
None of the ingredients of our product Scandonest® 3% plain are an evident source of alcohol.
None of the ingredients of our product Scandonest® 3% plain are an evident source of gluten.
None of the ingredients of our product OraVerse™ are an evident source of peanut, soy or nut.
None of the ingredients of our product OraVerse™ are an evident source of alcohol.
None of the ingredients of our product OraVerse™ are an evident source of gluten.
None of the ingredients of our product Marcaine® are an evident source of peanut, soy or nut.
None of the ingredients of our product Marcaine® are an evident source of alcohol.
None of the ingredients of our product Marcaine® are an evident source of gluten.
None of the ingredients of our product Lignospan® standard are an evident source of peanut, soy or nut.
None of the ingredients of our product Lignospan® standard are an evident source of alcohol.
None of the ingredients of our product Lignospan® standard are an evident source of gluten.
None of the ingredients of our product Lignospan® forte are an evident source of peanut, soy or nut.
None of the ingredients of our product Lignospan® forte are an evident source of alcohol.
None of the ingredients of our product Lignospan® forte are an evident source of gluten.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:50,000 are an evident source of peanut, soy or nut.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:50,000 are an evident source of alcohol.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:50,000 are an evident source of gluten.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:100,000 are an evident source of peanut, soy or nut.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:100,000 are an evident source of alcohol.
None of the ingredients of our product Cook-Waite Lidocaine HCl 2% and Epinephrine 1:100,000 are an evident source of gluten.
Our product Scandonest 30 mg/mL does not contain vasoconstrictor.
None of the ingredients of our product Carbocaine® 3% are an evident source of peanut, soy or nut.
None of the ingredients of our product Carbocaine® 3% are an evident source of alcohol.
None of the ingredients of our product Carbocaine® 3% are an evident source of gluten.
None of the ingredients of BioRoot RCS are an evident source of gluten.
None of the ingredients of BioRoot RCS are an evident source of iodine.
BioRoot RCS is composed of a powder and an aqueous solution. The powder is based on tricalcium silicate, zirconium oxide and povidone. The aqueous solution is composed of calcium chloride and polycarboxylate.
A box of BioRoot RCS contains 35 applications.
BioRoot RCS has optimized working and setting times:
– Working time > 10 minutes
– Setting time < 4 hours
1) Put one spoonful of BioRoot RCS on a mixing pad
2) Add 5 drops of mixing solution
3) Mix until obtention of a homogeneous paste (approx. 60 seconds)
4) Use the paste immediately after mixing
None of the ingredients of BioRoot Flow are an evident source of iodine.
None of the ingredients of BioRoot Flow are an evident source of gluten.
BioRoot Flow is composed of tricalcium silicate, propylene glycol, povidone, calcium carbonate, Aerosil (silica), zirconium oxide, acrylamide / sodium acryloyldimethyltaurate copolymer, isohexadecane and polysorbate.
None of the ingredients of Biodentine XP are an evident source of gluten.
The Biodentine® XP powder component is composed of:
The Biodentine® XP liquid component is composed of:
Both the powder and liquid components are included in the Biodentine® XP capsule and are ready to mix.
None of the ingredients of Biodentine are an evident source of gluten.
Depending on the desired application, Biodentine® can be placed with an amalgam carrier, a spatula (different from the one supplied in the box), or a Messing Root Canal Gun.
Biodentine® needs to be mixed at high speed and strength, and should only be mixed in a triturator/amalgamator. Mixing by hand may result in inconsistent material properties, potentially affecting setting and sealing. It can also introduce air into the material, which may reduce its mechanical strength. Further, Biodentine® has a working time of six minutes; mixing by hand is slower and can significantly reduce the time available to handle and place the material.
To ensure proper mixing, Biodentine® should always be mixed using a triturator/amalgamator. Examples of compatible products can be found in the Biodentine® instructions for use.
The aqueous solution is composed of calcium chloride and polycarboxylate.
The powder is composed of tricalcium silicate, zirconium oxide, calcium oxide, calcium carbonate and iron oxides pigment.
Yes, BioRoot Flow also provides high performance and safety.
A syringe of BioRoot Flow contains 15 to 20 applications.
Yes, BioRoot Flow can be used with all the obturation techniques, both warm and cold.
Biodentine is creamy, white color.
Yes, Biodentine® can be placed directly over the pulp. Thanks to the high purity of the tricalcium silicate material and the absence of contaminants such as heavy metals, Biodentine® is a biocompatible medical device, without mutagenic, irritant, or sensitizing potential. Internal studies and clinical experience highlighted that Biodentine® is very well tolerated by the pulp tissue. Moreover, thanks to its bioactivity*, it promotes a favorable environment for angiogenesis and osteogenesis, thus stimulating the healing process3.
* properties verified by preclinical studies
The setting time is in average 12 min after the mix.
No, to ensure the best consistency, Biodentine XP 200/500 has to be mixed with our tailor-made mixer extruded with the Biodentine® Gun. Otherwise, its technical specifications are not guaranteed. The patented, high-speed mixer is tailor-made for Biodentine® XP cartridges, designed to mix the cartridge and provide the required consistency in 30 seconds.
Biodentine® XP is applied directly into the tooth using the Biodentine® XP Dispenser Gun. Once mixed, slot the Biodentine® XP cartridge into the gun and bend the flexible nozzle to the suitable angle for accessing the tooth. Then simply place the nozzle into the cavity and squeeze the handle of the gun for direct application into the tooth for crown indications. Alternatively, you may apply Biodentine® XP with an amalgam carrier, a spatula, or a Root Canal Messing Gun. If necessary, the material can be manipulated and shaped using hand instruments during its working time of approximately six minutes.
It takes just 30 seconds to mix the Biodentine® XP cartridge to the required consistency using the high-speed Biodentine® XP Mixer.
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