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1.1 ml 3 syringes
How to use
Should be performed by a certified professional.
Store in 2 – 25°C. Protect from direct sunlight and freezing
T.A Bio Tech Co., Ltd.
Performance: Hyaluronic acid is a high molecular substance composed of repeated disaccharides of N-acetyl glucosamin and glucuronic acid. Zentia has realized a stable gel through precision cross-linking technology. The stable stucture of hyaluronic acid gel fills the space, supports the structure, protects the cell, replenishes the volume of wrinkled skin and keeps it natural.
Safety: The active ingredient used in Zentia is non-animal. It is a human-adapted component, contains high-purity hyaluronic acid and naturally decomposed over time. Hyaluronic acid cross-linking gel can be corrected through hyaluronidase when a problem occurs. It is safe by providing the level of endotoxin and crosslinking agent below the detection limit through strict manufacturing process management.
Usability: Precisely designed handles and push rods keep the pressure at the time of injection evenly, enabling stable treatment. The monophasic structure is a regular and stable gel structure, and it is a specialized technology applied to Zentia that realizes natural volume and soft injection feeling.
Pain relief: Zentia contains Lidocaine to improve pain-related discomfort during the treatment.
|Mid to deep dermis
|Mid to deep dermis subcutaneous layer
|24 mg / ml
|Nasolabial folds, forehead, marionette lines and face lifting
|Facial contouring, chin and chick augmentation
|1.1ml * 3syr
|Store in 2 – 25°C. Protect from direct sunlight and freezing
The durations are depends on age, lifestyle and the skill of a practitioner.
Zentia is manufactured using 100% authentic high-quality hyaluronic acid, every Finished product complies with European Pharmacopoeia on the endotoxin level.
Test items – Endotoxin. Acceptance Criteria – Not more than 12.5 EU/ml. Results – Less than 0.5 EU/ml
10 steps only Zentia’s unique manufacturing technology enables high elasticity with lower amount of cross-linking agent and residual BDDE
Test items – BDDE. Acceptance Criteria – <2ppm (NMT 2ppm). Results – Not detected
No swelling, no break during injection, maintaining original shape and natural look. Keep shape after injection. Not easily broken by water
Test items – Viscosity (Apparent viscosity, 50Hz). Acceptance Criteria – 13100cp~ 17000cp. Results – 16000cp
Test items – Extrusion force. Acceptance Criteria – Not more than 25N. Results – 10N
High HA concentration;
Safety Raw materials;
No residual BDDE;