Evaluation of the Efficacy and Safety of an Injectable Hyaluronic Acid-based Filler, Art Filler® Volume: Comparative Single-blind Study of the Non-inferiority Versus Juvéderm® Voluma on the Midface, Temple and Jaw-line and Non-comparative Study on the Chin. (AF3)

Inclusion Criteria: 1. Subjects who had signed a written informed consent 2. Man or Woman with an age ≥ 19 years old 3. Subject having a Fitzpatrick Phototype I to IV (annex 6) 4. Subject having a score of ≥ 2 in Global aesthetic 6-point scale scoring system on at least one area of interest (chin, midface, temples or jaw lines) (annex 1.1) 5. Subject having at least one of the following scales by clinical scoring (annex 1.2/1.3/1.4/1.5) * a grade of 2 or 3 on the ACRS Scale * a grade of 2 or 3 score on the MMVS Scale * a grade of 2 or 3 or 4 score on ATHS Scale * a grade of 2 or 3 score with NCJLS Scale 6. Subject registered with health insurance regimen 7. Woman agreeing to take a pregnancy test Exclusion Criteria: 1. Subject currently participating in another clinical study related to pharmaceuticals or medical devices or being in exclusion period of another clinical study. 2. Subject deprived of freedom by an administrative or legal decision 3. Subject who have received indemnification of 4500 € during the 12 previous months for his/her participation in clinical trials (including his participation in this study). 4. Subject who had facial injections/implants of any non-absorbable fillers in her/his whole life. 5. Subject who had laser sessions for skin rejuvenation or a laser resurfacing during the 12 previous months or a surgical facelift during the 2 years before the study. 6. Subject with a history of facial aesthetic injection (hyaluronic acid within the previous year, botulinum toxin within the last 6 months and long-term temporary injectable implants (semi-permanent implants) within the previous 2 years). 7. Subject with a skin-retaining device on the face (mesh, gold wire, liquid silicone or other particulate material). 8. Subject who undergo a non-invasive rejuvenation method such as moderate to deep peeling, ultrasound, radiofrequency devices or lasers within the last 6 months. 9. Subject with a history of severe multiple allergies or anaphylactic shock. 10. Subject with a known hypersensitivity to hyaluronic acid, Lidocaine and/or other components of Art Filler® Volume and Juvéderm Voluma solutions. 11. Subject with a known hypersensitivity to chlorhexidine. 12. Subject with a known hypersensitivity to lidocaine or local amide anesthetics. 13. Subject tending to develop inflammatory skin diseases or hypertrophic scars. 14. Subject with a history of streptococcal disease (recurring angina, rheumatic fever). 15. Subject with oral or injectable corticoid treatment (or not stopped for at least 3 months). Inhaled corticoids are permitted as well as topical corticotherapy not involving the head or the neck. 16. Subjects with any concomitant treatment (or not stopped for at least a year) by immunosuppressant or chemotherapy. 17. Subject with a history of radiotherapy involving the head and the neck within the previous year. 18. Subject with a history or a disease associated to the autoimmune or connective tissue disease. 19. Subject presenting at his/her face and/or neck any skin disease, or an acute inflammatory reaction or a bacterial/viral infection or who had such an episode within the previous 6 weeks. 20. Subject who took aspirin or anticoagulants at regular doses in the last 15 days prior to the act. 21. Subject who has permanently been exposed to the sun or the UV during the last 15 days. 22. Subject with dermatological condition or inflammation on or near the area to be treated (according to the opinion of the investigator). 23. Pregnant or lactating woman. 24. Subject with epilepsy not controlled by treatment.