REGENOVUE Deep Plus with Lidocaine

REGENOVUE Deep Plus is a professional cross-linked hyaluronic acid dermal filler with lidocaine. Supplied as one sterile 1.1ml prefilled syringe, it has a medium gel profile intended for qualified professional assessment of suitable lower-dermis and upper-subcutaneous facial applications.

The formulation contains 24mg/ml of cross-linked hyaluronic acid and 0.3% lidocaine. The incorporated lidocaine is intended to improve patient comfort during administration. REGENOVUE Deep Plus is manufactured in South Korea by NeoGenesis Co., Ltd.

REGENOVUE Deep Plus must only be purchased and administered by appropriately qualified, trained and insured healthcare or aesthetic professionals.

What Is REGENOVUE Deep Plus Used For?

REGENOVUE Deep Plus is the medium-profile, lidocaine-containing filler in the REGENOVUE Plus range. Manufacturer product information positions it for professional lower-dermis and upper-subcutaneous placement where a balanced combination of softness and support is required.

Depending on the patient’s anatomy, tissue characteristics and clinical assessment, a qualified practitioner may consider REGENOVUE Deep Plus for selected moderate facial folds, nasolabial folds, lips, chin or cheek treatments. These are general product-positioning examples rather than treatment recommendations for every patient.

The treating professional must determine whether this product, the intended treatment area, placement depth, quantity and technique are appropriate following an individual consultation and risk assessment.

REGENOVUE Deep Plus Product Specifications

Product: REGENOVUE Deep Plus with Lidocaine
Product type: Cross-linked hyaluronic acid dermal filler
Hyaluronic acid concentration: 24mg/ml
Lidocaine concentration: 0.3% or 3mg/ml
Formulation: Monophasic cross-linked hyaluronic acid gel
Presentation: One 1.1ml prefilled syringe
Recommended professional positioning: Lower dermis or upper subcutaneous tissue
Needles: Two 27G sterile needles, subject to supplied packaging
Manufacturer: NeoGenesis Co., Ltd.
Country of manufacture: South Korea
Storage: 2°C to 25°C, protected from direct sunlight
Use: Professional aesthetic use only

Always check the physical carton to confirm the exact syringe volume, accessory configuration, batch number, expiry date and current manufacturer instructions before treatment or publication.

Key Features of REGENOVUE Deep Plus

Professional cross-linked hyaluronic acid dermal filler
Contains 24mg/ml hyaluronic acid
Contains 0.3% lidocaine
Medium gel profile for suitable lower-dermis applications
Supplied as a sterile 1.1ml prefilled syringe
Part of the REGENOVUE Plus lidocaine-containing range
Manufactured by NeoGenesis in South Korea
Requires individual patient assessment and informed consent

Cross-Linked Hyaluronic Acid

Hyaluronic acid is naturally present within the human body and contributes to tissue hydration and structure. In a dermal filler, cross-linking creates a gel that can provide temporary physical support when correctly placed in suitable tissue by a qualified professional.

REGENOVUE Deep Plus has a more supportive profile than REGENOVUE Fine Plus, while remaining less robust than REGENOVUE Sub-Q Plus. Product selection should be based on tissue depth, facial anatomy, movement in the treatment area, the level of support required and the practitioner’s professional judgement.

Hyaluronic acid fillers are not permanent implants. Treatment response and visible duration can vary according to placement, quantity, treatment area, individual metabolism, lifestyle and tissue characteristics. No particular result or duration can be guaranteed.

REGENOVUE Deep Plus Compared with Other REGENOVUE Fillers

REGENOVUE Fine Plus: Fine gel profile for suitable upper-dermis applications.
REGENOVUE Deep Plus: Medium gel profile for suitable lower-dermis and upper-subcutaneous applications.
REGENOVUE Sub-Q Plus: Larger-particle gel profile for suitable deep-support applications.

The “Plus” designation identifies REGENOVUE products containing lidocaine. The appropriate product should be selected according to individual anatomy, intended treatment area, tissue depth and required support—not simply according to the severity of a visible line.

Professional Consultation and Patient Assessment

Before using REGENOVUE Deep Plus, the practitioner should review the patient’s medical history, allergies, medication, previous aesthetic procedures, skin condition and treatment expectations. The intended treatment area should be assessed for infection, inflammation, irritation, broken skin or another factor that could make treatment unsuitable.

Patients should receive clear information about the planned treatment, realistic limitations, possible adverse effects, aftercare and alternative options. Informed consent should be obtained before treatment. Product traceability details, including batch number and expiry date, should be documented in the patient record.

Important Safety Information

REGENOVUE Deep Plus must never be injected into a blood vessel. Accidental intravascular administration of any dermal filler can cause serious complications, including vascular occlusion, tissue damage, skin necrosis, visual impairment, blindness or stroke.

Administration requires detailed facial-anatomy knowledge, aseptic technique and the ability to recognise and manage complications promptly. Qualified practitioners should maintain appropriate emergency procedures, equipment and referral arrangements.

Do not use REGENOVUE Deep Plus in patients with known hypersensitivity to hyaluronic acid, lidocaine, amide-type local anaesthetics or another product component. Do not treat areas affected by active infection, inflammation, irritation, broken skin, untreated skin disease or an active cold-sore outbreak.

Pregnancy, breastfeeding, immune conditions, anticoagulant medication, bleeding disorders, significant allergies, recent treatment in the same area and a history of problematic scarring require careful professional consideration. Review the supplied manufacturer instructions before use.

Possible Treatment Reactions

Temporary injection-site reactions may include redness, swelling, tenderness, bruising, itching, firmness, discomfort or discolouration. Less common complications can be serious and may require urgent professional assessment.

Patients should receive written aftercare information and clear contact instructions. Unexpected or increasing pain, skin blanching, unusual colour changes, visual symptoms or neurological symptoms require immediate professional attention.

Storage, Handling and Traceability

Store REGENOVUE Deep Plus at 2°C to 25°C and protect it from direct sunlight unless the supplied carton states otherwise. Do not use the product if its sterile packaging is damaged, the expiry date has passed, the gel appears abnormal or storage conditions cannot be verified.

The prefilled syringe and supplied needles are single-use devices. Do not reuse or resterilise them. Dispose of used equipment and unused product through appropriate clinical and sharps-waste procedures.

Order REGENOVUE Deep Plus

REGENOVUE Deep Plus with Lidocaine is available from The Clinic Vault for eligible professional purchasers. Customers are responsible for ensuring that they have the qualifications, training, insurance and legal authority required to purchase and administer injectable aesthetic products.

Explore our professional aesthetic product collection or review available REGENOVUE product information before procurement.

Professional-use notice: This page provides product-identification and professional-procurement information only. It does not replace supplied manufacturer instructions, accredited clinical training, local regulations, professional judgement or an individual patient assessment.

REGENOVUE Deep Plus

REGENOVUE Deep Plus with Lidocaine 1.1ml