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Bonetta Volume
Bonetta Volume is a high-performance hyaluronic acid dermal filler (24 mg/ml HA + 0.3% lidocaine) for deep wrinkle correction (87% improvement in nasolabial folds), lip augmentation (92% patient satisfaction), and facial contouring. Its high cross-linking technology ensures 12-24 month longevity, while low-viscosity gel enables smooth injection (0.15N force) with 83% reduced edema risk.
$38.50
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 4% | $36.96 |
| 10-19 | 8% | $35.42 |
| 20-Unlimited | 10% | $34.65 |
Bonetta Volume HA Filler
Bonetta Volume is a stabilized hyaluronic acid dermal filler containing 24 mg/ml HA with 0.3% lidocaine. Utilizing high cross-linking technology, it demonstrates 78% higher elasticity than standard HA fillers, ensuring smooth injection and lasting results of 12-24 months. Clinical trials show 92% patient satisfaction in lip augmentation and 87% reduction in nasolabial fold depth at 6-month follow-up.
Long-lasting Effect
12-24 month duration with optimal tissue integration
Smooth Application
Low injection force (0.15N) minimizes edema risk
Pain Reduction
Integrated lidocaine ensures comfortable procedure
Fast Recovery
83% patients resume normal activity within 24 hours
Approved Indications
- Nasolabial folds & deep wrinkles (Glabella, Perioral, Mental)
- Facial volumization (Cheekbones, Jawline, Chin)
- Lip augmentation (Vertical lines, Border definition)
- Non-surgical rhinoplasty (Dorsum correction)
Product Specifications
Storage: 2-25°C in original package. Avoid freezing.
Shelf Life: 24 months unopened
Clinical Protocol
- Inject into deep dermis/subcutaneous tissue using linear threading
- Recommended depth: 2.5-4mm depending on treatment area
- Contraindicated in patients with severe allergies or active skin infections
- Post-treatment: Apply cold compress, avoid pressure/massage
Important Notice
Results may vary based on individual tissue response and injection technique.
For medical professional use only. Not for self-administration.
Proper patient screening and injection training are mandatory. Report adverse events to local health authority.
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