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RENEFIL LIGHT PLUS
Name: RENEFIL LIGHT PLUS
Manufacturer: BMI Korea
Active Substance(s): POLYDEOXYRIBONUCLEOTIDE, HA, LIDOCAINE
Sku:100106
In Stock
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RENEFIL LIGHT PLUS Product Description
RENEFIL LIGHT PLUS is a hybrid dermal filler combining cross-linked hyaluronic acid (HA) with polynucleotides (PN) and lidocaine. Designed for superficial to mid-dermal injections, it targets fine lines, skin hydration, and texture improvement, making it suitable for early signs of aging or maintenance treatments.
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Type: Cross-linked HA + PN + Lidocaine
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Application: Reduces fine lines and improves skin smoothness
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Packaging: Supplied as a 1 mL prefilled syringe with 2 sterile needles
RENEFIL LIGHT PLUS Key Features and Benefits
RENEFIL LIGHT PLUS is engineered to deliver gentle yet effective improvements in skin quality, hydration, and fine wrinkle reduction. Its lower viscosity allows for smooth flow and even distribution in delicate facial zones.
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Improves hydration, brightness, and skin texture
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Effective in superficial lines without creating excess volume
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Provides skin support and stimulates collagen synthesis
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Contains lidocaine for reduced injection discomfort
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Suitable for early-stage aging or post-correction maintenance
RENEFIL LIGHT PLUS Composition
Each RENEFIL LIGHT PLUS syringe contains a standardized formulation optimized for hydration and fine line correction.
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Cross-Linked Hyaluronic Acid (HA) – 20 mg/mL
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Offers subtle volume and dermal hydration
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Sodium Polynucleotide (PN) – 1.875 mg/mL
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Stimulates fibroblast activity and collagen production
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Lidocaine HCl – 0.3% (3 mg/mL)
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Minimizes injection discomfort
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RENEFIL LIGHT PLUS Intended Purpose / Indications
RENEFIL LIGHT PLUS is designed to improve early signs of aging and maintain healthy, glowing skin by targeting fine lines and surface irregularities.
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Reduces perioral lines, glabellar lines, and fine forehead wrinkles
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Ideal for hydrating the skin, enhancing luminosity, and improving skin smoothness
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Can be used preventively in younger patients or as part of a skin rejuvenation protocol
RENEFIL LIGHT PLUS Injection and Treatment Areas
This filler is intended for superficial to mid-dermal administration. Its fine particle size allows safe and even injection in sensitive areas.
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Recommended for:
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Periorbital lines (crow’s feet)
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Perioral wrinkles (smoker’s lines)
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Glabellar lines (frown lines)
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Forehead wrinkles
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Neck and décolletage
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Injection depth: Superficial to mid-dermis
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Needle size: Typically 30G for precision and control
RENEFIL LIGHT PLUS Reconstitution and Preparation Guidelines
RENEFIL LIGHT PLUS is provided as a sterile, ready-to-use filler that requires no reconstitution or dilution before use.
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Supplied in a 1.0 mL colorless prefilled syringe
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Includes 2 individually packaged sterile needles
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Use immediately after opening
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Handle under aseptic conditions to maintain sterility
RENEFIL LIGHT PLUS Administration and Dosage
Treatment should be performed by qualified medical professionals trained in superficial dermal filler techniques.
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Inject slowly and evenly using linear threading or micro-aliquot techniques
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Typical dosage: 0.5–1.0 mL per session, depending on the treatment area
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Avoid overcorrection due to the product’s hydrating expansion effect
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Results may be visible after a single session, but multiple treatments may be used for optimal results
RENEFIL LIGHT PLUS Storage Instructions
Maintain optimal efficacy and safety by following recommended storage guidelines.
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Store between 2°C and 25°C (36°F to 77°F)
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Do not freeze or expose to direct sunlight
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Store in original packaging to protect from contamination
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Single-use product—discard any unused amount after the first use
RENEFIL LIGHT PLUS Contraindications
Do not administer RENEFIL LIGHT PLUS in the following conditions:
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Known hypersensitivity to HA, PN, or lidocaine
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Active skin infections or inflammation at the injection site
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Autoimmune diseases or chronic skin conditions
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Pregnancy or breastfeeding
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History of anaphylaxis or severe allergic reactions
RENEFIL LIGHT PLUS Precautions and Warnings
While safe for most patients, RENEFIL LIGHT PLUS requires careful handling and proper patient assessment.
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Avoid intravascular injection to prevent embolism
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Do not combine with abrasive cosmetic procedures (e.g., peels, laser) on the same day
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Use caution in areas with thin skin or low elasticity
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Only administer in clinical environments by trained personnel
RENEFIL LIGHT PLUS Post-Treatment Care
Patients should follow simple guidelines to minimize risk and enhance results.
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Avoid makeup, alcohol, and strenuous activity for at least 24 hours
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Refrain from saunas, hot baths, and UV exposure for 2–3 days
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Do not massage or press treated areas unless advised
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Apply cold compresses if minor swelling or bruising occurs
RENEFIL LIGHT PLUS Side Effects and Adverse Reactions
Most side effects are mild and resolve without intervention. Serious events are rare.
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Common side effects:
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Redness, swelling, pain, itching, or bruising at injection site
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Less common:
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Lumps, asymmetry, or discoloration
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Severe (rare):
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Intravascular complications, allergic reactions, or delayed granulomas
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Monitor and report any persistent or unusual reactions
RENEFIL LIGHT PLUS Patient Eligibility
The product is intended for adult patients who want to improve mild skin aging or maintain skin quality.
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Suitable for patients aged 18 and older
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Especially useful in younger individuals for preventive care
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Not recommended for patients with autoimmune, hematologic, or chronic inflammatory diseases
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Medical evaluation and informed consent are essential prior to use
RENEFIL LIGHT PLUS Follow-Up and Maintenance
RENEFIL LIGHT PLUS may require maintenance sessions to sustain results, particularly in mobile or superficial areas.
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Initial effects last approximately 6–9 months
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For optimal results, repeat treatments every 6–12 months depending on patient’s metabolism and area treated
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Follow-up sessions help maintain skin hydration and fine line reduction
RENEFIL LIGHT PLUS Manufacturer and Regulatory Information
RENEFIL LIGHT PLUS is manufactured by BMI Korea Co., Ltd., and conforms to international medical device safety standards.
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Manufacturer: BMI Korea Co., Ltd., Jeju, Republic of Korea
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Regulatory Status: CE-certified
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CE Certificate Number: 2020-MDD/05-095
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Produced under EN ISO 13485:2016 quality management system
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Patent-protected formulation combining HA and PN
RENEFIL LIGHT PLUS FAQ
Is this filler only for wrinkles?
No. It also hydrates the skin, improves texture, and boosts radiance.
Is it painful to inject?
No. It contains 0.3% lidocaine to make injections more comfortable.
How long do results last?
Effects typically last 6–9 months, depending on skin type and lifestyle.
Can it be used on younger patients?
Yes. It is safe and effective for preventive care in individuals 18+.
What makes this different from deeper fillers?
It is optimized for fine lines, surface hydration, and non-volumizing skin improvement.
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