Dermal Fillers
REVANESSE references stocked by ALLPARA for professional use, sourced direct and certified on every shipment.
CE Marked
SKU 11110
Revanesse Contour™+
In stock
Volume
2 x 1,2 mL
Laboratory
Prollenium Medical Technologies Inc.
Origin
Canada
Indication
Facial volume enhancement and contouring
Trade price and history are verified-only
allpara supplies licensed practitioners. Sign in or apply for a B2B account to see live pricing, volume tiers and price history.
Revanesse Contour+ is a colourless, odourless, transparent aqueous gel of synthetic origin from Prollenium Medical Technologies in Aurora, Canada. It carries cross-linked hyaluronic acid at 25 mg/mL with lidocaine at 3 mg/mL (0.3% w/w) in phosphate-buffered saline, cross-linked with BDDE. Its application range is medium to deep facial rhytides, and its cosmetic indication covers facial rhytides, volume restoration, lip augmentation, skin hydration and the contouring of depressions by injection into tissue. It is supplied as two pre-filled 1.2 mL syringes with up to two sterilised needles, and is for intradermal use only.
Key Benefits of Revanesse Contour™+
- Cross-linked hyaluronic acid 25 mg/mL with lidocaine 3 mg/mL for injection comfort
- Indicated for medium to deep facial rhytides
- Covers volume restoration, lip augmentation, skin hydration and contouring of depressions
- Also indicated for volume lost to lipoatrophy or lipodystrophy, including HIV-associated cases
- Supplied as two pre-filled 1.2 mL syringes with up to two sterilised needles
- CE marked 0653 for the syringe, with CE 0123 needles
Indications and Professional Use
Main indications
- Medium to deep facial rhytides
- Restoration of volume lost from lipoatrophy or lipodystrophy
- Correction of contour deficiencies and anatomic deformities of the facial soft tissue, of pathologic origin or after trauma
- Volume restoration
- Lip augmentation
- Skin hydration
- Contouring of depressions
Professional use
For professional use. Revanesse Contour+ should only be injected by or under the direct supervision of qualified physicians trained in the proper injection technique for filling facial wrinkles, and is not for retail sale or self-administration. The area must be thoroughly disinfected and injection performed under sterile conditions. Bring the product to room temperature for 30 minutes before injection, prime the syringe until a small drop appears at the needle tip, then inject slowly with the least pressure necessary. If the skin blanches, stop immediately and massage until normal colour returns. It must not be injected into an area already containing another filler or a permanent implant, must never be used for breast enlargement or implantation into bone, tendon, ligament or muscle, and must not contact quaternary ammonium salts such as benzalkonium chloride.
Treatment areas
- Facial soft tissue
- Lips
Patient profile
Intended for patients desiring correction of contour deficiencies and deformities in facial soft tissue, including HIV-associated lipoatrophy and lipodystrophy. It is contraindicated in hypersensitivity to any amide-type local anaesthetic, not only lidocaine, and in all degrees of atrioventricular block, sinus node dysfunction, severe decline in myocardial contractility, porphyria and supraventricular tachycardias. It must not be used in pregnancy or lactation, in anyone under 18, in patients who develop hypertrophic scarring, in patients with acne or other inflammatory skin disease, acute or chronic skin disease at or near the injection site, auto-immune disorders or immunotherapy, multiple severe allergies, coagulation defects or anti-coagulation therapy, sensitivity to hyaluronic acid, or unattainable expectations. It contains trace amounts of gram-positive bacterial proteins and is contraindicated in patients allergic to such material. Safety in patients over 65 has not been established.
How Revanesse Contour™+ Works
Contour+ is a space-occupying tissue reconstructive material: the cross-linked hyaluronic acid gel occupies volume in the facial soft tissue where it is placed, correcting contour deficiencies rather than acting on the tissue biologically. Its medical indication is the restoration of volume lost from lipoatrophy or lipodystrophy and the correction of contour deficiencies and anatomic deformities, whether of pathologic origin or following trauma. The lidocaine at 0.3% is present for injection comfort, which is also why hypersensitivity to amide-type anaesthetics is an outright contraindication rather than a caution.
Why Order From Allpara
Allpara offers genuine, verified REVANESSE products from vetted suppliers, with full batch-traceability and expert support. We serve clinics and aesthetic professionals with CE-certified products, fast EU-wide delivery from our EU warehouse, and competitive trade pricing. Our focus is your patients' safety, satisfaction and results - with dedicated after-sales support for your peace of mind.
Frequently Asked Questions
How does Contour+ differ from the rest of the Revanesse range?
Concentration and reach. Contour+ carries 25 mg/mL cross-linked hyaluronic acid with lidocaine and is indicated for medium to deep facial rhytides, extending to volume restoration, lip augmentation and the contouring of depressions. Renew+ sits at 14 mg/mL for skin-level treatment lasting around 4 weeks, while Sculpt+ shares the 25 mg/mL concentration but is placed in the middle dermis.
What should a practitioner do if the skin blanches during injection?
Stop the injection immediately and massage the area until the skin returns to its normal colour. Blanching can signal intravascular placement, which has been associated with embolisation, vision impairment, blindness, skin necrosis and stroke. Any patient showing changes in vision, signs of stroke or unusual pain during or shortly after the procedure needs prompt medical attention.
Is there a limit on how much can be injected in a year?
Yes. Based on a toxicological risk assessment for lidocaine, patients should be limited to 20 mL per 60 kg of body mass per annum. The safety of injecting greater amounts has not been established.
Where can clinics buy Revanesse Contour+?
ALLPARA supplies Revanesse Contour+ to licensed practitioners, clinics and distributors on a B2B account. Wholesale terms, stock position and batch expiry are released to registered professional buyers.
More from Prollenium Medical Technologies
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Revanesse Contour™+
In stock
CE Marked
Revanesse Contour+ is a colourless, odourless, transparent aqueous gel of synthetic origin from Prollenium Medical Technologies in Aurora, Canada. It carries cross-linked hyaluronic acid at 25 mg/mL with lidocaine at 3 mg/mL (0.3% w/w) in phosphate-buffered saline, cross-linked with BDDE. Its application range is medium to deep facial rhytides, and its cosmetic indication covers facial rhytides, volume restoration, lip augmentation, skin hydration and the contouring of depressions by injection into tissue. It is supplied as two pre-filled 1.2 mL syringes with up to two sterilised needles, and is for intradermal use only.
Key Benefits of Revanesse Contour™+
- Cross-linked hyaluronic acid 25 mg/mL with lidocaine 3 mg/mL for injection comfort
- Indicated for medium to deep facial rhytides
- Covers volume restoration, lip augmentation, skin hydration and contouring of depressions
- Also indicated for volume lost to lipoatrophy or lipodystrophy, including HIV-associated cases
- Supplied as two pre-filled 1.2 mL syringes with up to two sterilised needles
- CE marked 0653 for the syringe, with CE 0123 needles
Indications and Professional Use
Main indications
- Medium to deep facial rhytides
- Restoration of volume lost from lipoatrophy or lipodystrophy
- Correction of contour deficiencies and anatomic deformities of the facial soft tissue, of pathologic origin or after trauma
- Volume restoration
- Lip augmentation
- Skin hydration
- Contouring of depressions
Professional use
For professional use. Revanesse Contour+ should only be injected by or under the direct supervision of qualified physicians trained in the proper injection technique for filling facial wrinkles, and is not for retail sale or self-administration. The area must be thoroughly disinfected and injection performed under sterile conditions. Bring the product to room temperature for 30 minutes before injection, prime the syringe until a small drop appears at the needle tip, then inject slowly with the least pressure necessary. If the skin blanches, stop immediately and massage until normal colour returns. It must not be injected into an area already containing another filler or a permanent implant, must never be used for breast enlargement or implantation into bone, tendon, ligament or muscle, and must not contact quaternary ammonium salts such as benzalkonium chloride.
Treatment areas
- Facial soft tissue
- Lips
Patient profile
Intended for patients desiring correction of contour deficiencies and deformities in facial soft tissue, including HIV-associated lipoatrophy and lipodystrophy. It is contraindicated in hypersensitivity to any amide-type local anaesthetic, not only lidocaine, and in all degrees of atrioventricular block, sinus node dysfunction, severe decline in myocardial contractility, porphyria and supraventricular tachycardias. It must not be used in pregnancy or lactation, in anyone under 18, in patients who develop hypertrophic scarring, in patients with acne or other inflammatory skin disease, acute or chronic skin disease at or near the injection site, auto-immune disorders or immunotherapy, multiple severe allergies, coagulation defects or anti-coagulation therapy, sensitivity to hyaluronic acid, or unattainable expectations. It contains trace amounts of gram-positive bacterial proteins and is contraindicated in patients allergic to such material. Safety in patients over 65 has not been established.
How Revanesse Contour™+ Works
Contour+ is a space-occupying tissue reconstructive material: the cross-linked hyaluronic acid gel occupies volume in the facial soft tissue where it is placed, correcting contour deficiencies rather than acting on the tissue biologically. Its medical indication is the restoration of volume lost from lipoatrophy or lipodystrophy and the correction of contour deficiencies and anatomic deformities, whether of pathologic origin or following trauma. The lidocaine at 0.3% is present for injection comfort, which is also why hypersensitivity to amide-type anaesthetics is an outright contraindication rather than a caution.
Why Order From Allpara
Allpara offers genuine, verified REVANESSE products with full batch-traceability, CE-certified stock, fast EU-wide delivery and expert after-sales support.
Frequently Asked Questions
How does Contour+ differ from the rest of the Revanesse range?
Concentration and reach. Contour+ carries 25 mg/mL cross-linked hyaluronic acid with lidocaine and is indicated for medium to deep facial rhytides, extending to volume restoration, lip augmentation and the contouring of depressions. Renew+ sits at 14 mg/mL for skin-level treatment lasting around 4 weeks, while Sculpt+ shares the 25 mg/mL concentration but is placed in the middle dermis.
What should a practitioner do if the skin blanches during injection?
Stop the injection immediately and massage the area until the skin returns to its normal colour. Blanching can signal intravascular placement, which has been associated with embolisation, vision impairment, blindness, skin necrosis and stroke. Any patient showing changes in vision, signs of stroke or unusual pain during or shortly after the procedure needs prompt medical attention.
Is there a limit on how much can be injected in a year?
Yes. Based on a toxicological risk assessment for lidocaine, patients should be limited to 20 mL per 60 kg of body mass per annum. The safety of injecting greater amounts has not been established.
Where can clinics buy Revanesse Contour+?
ALLPARA supplies Revanesse Contour+ to licensed practitioners, clinics and distributors on a B2B account. Wholesale terms, stock position and batch expiry are released to registered professional buyers.
More from Prollenium Medical Technologies
View laboratory →* Professional-use product. Packaging may vary by batch or market. Refer to the supplied IFU for full directions and contraindications.