CLOSING THE GAP
IN YOUR PRACTICE

Tone The Muscles To Address Lower Lid Laxity And Impaired Blinking With The New OptiLIFT™ Device

A woman with bright red hair looking upward

LIFT UP YOUR PRACTICE WITH LUMENIS’ INNOVATIVE DEVICE

Address Lower Lid Laxity and Impaired Blinking

By strengthening the muscles in the periorbital area, OptiLIFT addresses the gravitational descent of the lower lids that can result in ineffective blinking

Proprietary Dynamic Muscle Stimulation Technology

Lumenis’ DMSt uses electrical pulses to trigger nerve signals, activating facial muscles and inducing contractions

Ideal Fit For
Eye Practice

OptiLIFT applicator is specifically designed for the periorbital area, featuring three predefined presets for treating patients’ delicate facial contours

Clinically
Validated

OptiLIFT is easy-to-use, safe and clinically validated to address blinking and lower lid laxity

Tone and Tighten the Periorbital Muscles

OptiLIFT stimulates the muscles with DMSt technology to tone and tighten the periorbital area, targeting the natural sagging that comes with aging

THE POWER OF
OPTILIFT TECHNOLOGY

Non-Surgical Device to Tone Muscles to Address Droopy Eyelids

Aging weakens periorbital muscles, often leading to eyelid laxity, reduced tone and impaired blinking. OptiLIFT’s Dynamic Muscle Stimulation (DMSt) activates muscle contractions, enhances tone, and addresses both the function and appearance of the lower eyelids.

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TONE THE MUSCLES
BEFORE & AFTER

OptiLIFT delivers impressive and visible outcomes in just four easy sessions. It restores the tightness and tone of the muscle and enhances blinking efficiency, offering a gentle, non-invasive approach for a lifted appearance.

Courtesy of Dr. Dorina Cheles

CLINICALLY PROVEN TO ELEVATE YOUR PRACTICE

OptiLIFT is clinically validated1, with Dynamic Muscle Stimulation technology applied below the eyelids delivering results such as:

  • 286% improvement in tear breakup time (TBUT)
  • 70% Improvement in blinking rate and quality
  • Decrease of at least 75% in lower lid laxity
  • Enhanced meibomian gland function, improving signs of DED

WHAT DOCTORS
ARE SAYING

** The testimonials of the OptiLIFT believers and the providers represent specific experience of a paid spokesperson. The experience of other people may vary.

A PARTNERSHIP
YOU CAN TRUST

Experience the Lumenis Advantage & Build Your Future.
Partner with the pioneers who revolutionized dry eye care. Lumenis is your trusted partner for professional growth, clinical excellence, and expanding your practice—delivering innovative solutions that have been setting the gold standard in eye care for over 50 years.

DOWNLOAD INFO KIT

Discover how OptiLIFT can transform your practice.
Contact us for a free demo or to learn more!

1 Data on file; manuscript under preparation

Indication for use:
The OptiLIFT System and its accessories are intended for dermatological procedures requiring ablation and resurfacing of the skin when using VoluDerm Energy (Microneedling Applicator). It is also intended for use in dermatologic and general surgical procedures for non-invasive treatment when using RF Energy and for muscle conditioning to stimulate healthy muscles (OptiLIFT Applicator). OptiLIFT System is not intended to be used in conjunction with therapy or treatment of medical diseases or medical conditions of any kind. OptiLIFT System is intended to be operated by a trained professional who is present to monitor treatment.

Warnings and risks:
OptiLIFT System is contraindicated for patients with pacemakers, defibrillators, any implanted electronic device, or metal implanted in the treatment area.
Side effects may appear either at the time of treatment or shortly after. Side effects may include any of the following: prolonged or significant pain, damage to natural skin texture (blister, burn), excessive skin redness (erythema), excessive swelling (edema), fragile skin bruising, excessive itching, change of pigmentation (hyper-pigmentation or hypopigmentation), scarring transient skin break-out such as acne and pimples. For a complete list of contraindications, please refer to the User Manual.

PB-00086860, Rev A.