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FemTouch

Also known as: FemTouch, FemTouch Laser, FemTouch Vaginal Rejuvenation, Lumenis FemTouch, Fractional CO2 Vaginal Laser, Vaginal Fractional Laser Therapy, FemTouch CO2 Laser System, AcuPulse FemTouch, FemTouch Gynecological Laser, Vaginal Mucosa Resurfacing Laser, FemTouch Intimate Health Treatment, FemTouch Laser Vaginoplasty Alternative, CO2 Fractional Vaginal Rejuvenation, Lumenis Vaginal Laser Therapy, FemTouch Menopause Relief Laser

Intimate Rejuvenation

AI Aesthetician Summary

FemTouch is a revolutionary fractional CO2 laser treatment designed to address vaginal health concerns through non-surgical, non-hormonal vaginal rejuvenation. Developed by Lumenis, a leader in aesthetic medical lasers, this innovative technology offers a minimally invasive solution for women experi...

Treatment Details

Targets

Concerns:Vaginal DrynessVaginal Discolouration and Uneven LabiaVaginal LaxityWeak Pelvic Floor and Incontinence
Areas:Pelvis
Tissues:Skin (Epidermis, Dermis)
Longevity:1-2 Years

How it Works

Duration:30 minutes
Anesthesia:None
Pain Level:Mild
Techniques:Laser
Multiple Sessions:Yes

Post Treatment

Downtime:3 days
Post-care:Following FemTouch treatment, patients should generally refrain from sexual intercourse for 72 hours and avoid submerging the treated area in water (baths, hot tubs) or direct heat exposure for 2-3 days. While there is minimal downtime, mild swelling, discomfort, or itching can occur, which may be alleviated with cold compresses, over-the-counter pain relievers, or a prescribed hydrating gel.
Risks:Mild vaginal discharge or spotting (60-80% of patients, resolves in 1-3 days); transient discomfort or burning sensation during/after treatment (40-50%, managed without intervention); minor swelling or redness (20-30%, lasts 24-48 hours); low incidence of urinary urgency (10-15%, self-resolving); rare risks include infection (e.g., bacterial vaginosis, <1% with proper hygiene); thermal burns leading to scarring (0.5-1%, often due to improper settings); exacerbation of urinary incontinence if underlying severe prolapse present (<1%); allergic reaction to probe materials (extremely rare, <0.1%).

Additional Information

Invasiveness:Minimally Invasive
Manufacturer:Lumenis
Specialty:Cosmetic Surgery