OEM Custom Cross Linked Hyaluronic Acid Fillers Factories Exporter – Fine 1ml 2ml Hyaluronic Acid Dermal Filler for Remove Wrinkles – FLODERMA

Floderma cross-linked sodium hyaluronate injectable gel can enlarge the volume of subcutaneous tissue, It absorbs water from surrounding tissue to expand volume, then make the relaxation skin plump again . It can be used to treat and repair aging skin folds ,depression or scars and can also augment facial features such as cheeks and lips.It can also be used for therapeutic applications: correct the defects that result from medical disorders ,trauma,or surgery.And it can also fill the HIV-associated lipoatrophy ,scaring ,and surgical or traumatic skull defects,correct facial asymmetry (e.g. lip asymmetry after surgical correction of cleft lip). Floderma Fine can be injected into the dermis and effectively solve problems especially for static wrinkles, Such as the glabellas wrinkes ,crow’s feet ,lachrymals sulcus and nasolabial etc.

Treatment areas:
Ideal for in the periorbital region ,Shallow wrinkle remove ,as well as for modeling the following areas

E.g.

Crow’s feet
Corrects
Scars
Frown

Duration of effect:
As a result of the immediately visible results of treatment, there is an increase in the client’s self-esteem. The duration of the action can last 16-12 months. This depends on age, skin type, physical activity and technique used.

ADVERSE REACTIONS

Patients must be informed of the potential risks and adverse events related to the injection procedure and to the use of this product. A slight bleeding may occur during the injection, and it disappears spontaneously as soon as the injection is finished. In occasional cases one or more of the following may occur either immediately or as a delayed reaction (list not exhaustive) Reactions usually associated with injections such as redness, erythema, oedema or pain sometimes accompanied by itching in the treated area. These reactions may last for a week. Hematomas in the treated area, Swelling in the treated area, Indurations or nodules in the treated area, Coloration or discoloration in the treated area, Allergy to one of the product’s components, especially to sodium hyaluronate. Cases of necrosis, abscesses and granulomas after sodium hyaluronate injections have been reported in the literature.

These rare potential risks must nevertheless be considered. Patients should be instructed to report any side effects which last for more than one week to his/her practitioner.

The practitioner may then prescribe the patient appropriate treatment.

Any other undesirable side effects associated with injection of the product must be reported to the distributor and/or to the manufacturer.

Technique Information