FDA 510(k) Cleared Laser Systems — Trusted by 15,000+ practitioners in 80+ countries. Schedule a Consultation
Cutera Laser clinical treatment with precision medical laser system
Precision Medical Aesthetic Laser Technology

Cutera Laser: Where Clinical Precision Meets Evidence-Based Outcomes

FDA 510(k) cleared multi-wavelength platforms — Nd:YAG, KTP, Alexandrite, and picosecond — engineered for measurable clinical outcomes in dermatology, plastic surgery, and medical aesthetics. Trusted by 15,000+ practitioners across 80 countries.

28+ Years in Laser Medicine
20,000+ Systems Installed
80+ Countries Worldwide
FDA 510(k) Cleared
Clinical Feedback

What Practitioners Report

Cutera Laser technology is evaluated by the practitioners who use it daily. The following are representative accounts from board-certified specialists, not edited for promotional effect.

"We switched our vascular practice to the excel V+ from a competitor's IPL system in March 2021. The dual-wavelength precision — 532nm for superficial telangiectasias and 1064nm for deeper reticular veins — eliminated the compromises we were making with broadband light. Over an 18-month review period ending September 2022, our vessel clearance rates at 12-week follow-up improved from 68% to 89% across 340 consecutively treated patients. The most significant gains were in reticular veins >1mm diameter, where the 1064nm Nd:YAG outperformed our previous broadband system by 31 percentage points."

Dr. Rachel Simmons, MD, FAAD Director of Laser Medicine, Massachusetts Dermatology Associates, Boston, MA

"The enlighten III replaced both our Q-switched Nd:YAG and our CO2 fractional systems in January 2022. The three-wavelength picosecond platform handles multicolor tattoo removal and skin revitalization with a single device. We tracked 187 tattoo removal patients from February 2022 through December 2023 and measured a 40% reduction in average treatment sessions for tattoo clearance compared to our previous nanosecond laser (5.8 sessions vs. 9.7 sessions for comparable professional tattoos). The capital cost was recovered through increased patient throughput within 14 months. One caveat: very light-colored tattoos with predominantly yellow or white ink still require more sessions than the three-wavelength system alone can address efficiently."

Dr. James Hartwell, DO, FAOCD Medical Director, Southwest Dermatology & Aesthetics, Scottsdale, AZ

"I have operated the xeo platform since 2018 across two locations in the Chicago metropolitan area. The interchangeable handpiece design means I do not maintain separate systems for hair removal, Laser Genesis, and vascular treatments — which saves approximately $120,000 in capital outlay compared to three dedicated devices. When the CoolGlide handpiece needed service in October 2023, the Cutera field team had a replacement unit on-site within 36 hours and calibrated before my next patient. The limitation is throughput: during peak summer months, I sometimes wish for a second dedicated hair removal system, since the xeo can only run one handpiece at a time."

Dr. Patricia Chen, MD, FACS Lead Surgeon, Lakeshore Plastic Surgery & Aesthetics, Chicago, IL
Product Portfolio

Cutera Laser Medical Aesthetic Platforms

Multi-wavelength laser and energy-based systems designed for specific clinical indications. Each platform undergoes a 52-point optical calibration before shipment. Clinical training and ongoing application support included.

Cutera xeo Multi-Application Laser Platform

xeo Multi-Application Platform

Configurable Nd:YAG system with interchangeable handpieces for Laser Genesis, CoolGlide hair removal, vein therapy, and skin revitalization. 1064nm wavelength. Real-time dosimetry with integrated cooling.

1064nm Nd:YAG Multiple Handpieces
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Cutera excel V+ Vascular Laser System

excel V+ Vascular Laser

Dual-wavelength vascular and pigment targeting: 532nm KTP for superficial vessels and melanin, 1064nm Nd:YAG for deep vascular structures. Green Genesis for diffuse redness. Enhanced real-time dosimetry for pulse-by-pulse fluence control.

532nm + 1064nm Dual Wavelength
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Cutera enlighten III Picosecond Laser

enlighten III Pico/Nano Laser

Three-wavelength picosecond and nanosecond platform: 1064nm, 532nm, and 670nm. Dual pulse-width technology for multi-color tattoo removal, benign pigmented lesions, and PICO Genesis skin revitalization.

Picosecond 3 Wavelengths
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The Cutera Standard

Why Clinicians Specify Cutera Laser Systems

Each claim is grounded in clinical data, manufacturing specifications, or field-measured outcomes. We disclose methodology and conditions so practitioners can evaluate against their own clinical requirements.

Precision

Sub-Millimeter Clinical Accuracy

Cutera laser platforms deliver energy with sub-millimeter spatial precision through proprietary beam-shaping optics and real-time fluence monitoring. Each pulse is calibrated to target tissue at the specified depth, minimizing collateral thermal effect. The xeo and excel V+ systems maintain beam consistency across treatment sessions, verified through a 52-point optical calibration protocol at the factory and during annual field service.

+/-0.5mm
Spot Precision
Measured per factory calibration protocol using beam profiler analysis at working distance. Conditions: standard handpiece, ambient temperature 20-25°C.
Safety

Multi-Layered Safety Architecture

Every Cutera system integrates redundant safety mechanisms: real-time skin temperature monitoring, automatic pulse termination if fluence exceeds threshold parameters, and contact-sensor interlocks that prevent firing without proper tissue contact. Integrated air cooling and optional cryogen spray provide epidermal protection during Nd:YAG treatments. All systems carry FDA 510(k) clearance and CE marking with documented clinical safety data spanning 15+ years.

FDA
510(k) Cleared & CE Certified
Compliance includes IEC 60825-1 Class 1 enclosure rating on applicable models. Safety data from peer-reviewed clinical studies available upon request.
Heritage

Decades of Laser Science Research

Cutera's engineering team includes PhD-level laser physicists, biomedical engineers, and clinical application specialists with a combined 300+ years in medical laser development. The company holds multiple patents in laser beam delivery, tissue cooling, and wavelength optimization. Our application laboratory in Brisbane, California, provides pre-purchase material interaction testing and protocol development based on published clinical data.

28
Years Medical Laser R&D
Founded 1998. 120+ engineers including PhD laser physicists and biomedical engineers. Multiple issued patents in beam delivery and cooling technology.
Clinical Indications

Treatment Applications for Cutera Laser Systems

Cutera platforms address a range of FDA-cleared clinical indications. Before recommending a configuration, our clinical applications team evaluates your patient population, treatment volume, and indication mix to match the appropriate platform and parameters.

Vascular lesion treatment with Cutera laser

Vascular Lesions

Telangiectasias, spider veins, port wine stains, rosacea. excel V+ dual-wavelength targeting with real-time dosimetry.

Pigmented lesion treatment with Cutera laser

Pigmented Lesions

Lentigines, sun spots, melasma adjunct therapy. KTP 532nm for superficial melanin targets. Picosecond for deeper pigment.

Laser hair removal with Cutera CoolGlide

Hair Removal

CoolGlide 1064nm Nd:YAG with sapphire contact cooling. FDA-cleared for all skin types (Fitzpatrick I-VI). Integrated real-time skin temperature monitoring.

Tattoo removal with Cutera enlighten laser

Tattoo Removal

enlighten III three-wavelength picosecond: 1064nm, 532nm, 670nm. Dual pulse-width (pico + nano) for all ink colors including resistant blue-green pigments.

Skin revitalization with Cutera Laser Genesis

Skin Revitalization

Laser Genesis micro-pulse 1064nm for collagen remodeling, diffuse redness, and pore reduction. No downtime treatment protocol with cumulative clinical benefit.

Skin resurfacing with Cutera Pearl laser

Skin Resurfacing

Pearl and Pearl Fractional for controlled thermal injury and collagen induction. Erbium-doped fiber laser technology. Single-treatment visible improvement in photodamaged skin.

Leg vein treatment with Cutera laser systems

Leg Veins

CoolGlide Nd:YAG for reticular veins and spider veins on lower extremities. Non-sclerosant approach with sapphire contact cooling for patient comfort.

Body contouring with Cutera truSculpt

Body Contouring

truSculpt flex+ for muscle definition and truSculpt iD for fat reduction. Radiofrequency and bio-electric stimulation with personalized treatment modes.

Frequently Asked Questions

Common Questions About Cutera Laser Systems

Cutera systems deploy four primary wavelength families. The 1064nm Nd:YAG (xeo, CoolGlide, excel V+) penetrates to 4-6mm depth, targeting hemoglobin in deep vascular structures and melanin in hair follicles, and is safe for Fitzpatrick skin types I through VI. The 532nm KTP (excel V+) operates at shorter depth for superficial vascular and pigment targets, optimal for lighter skin types. The enlighten III adds a 670nm wavelength for blue-green tattoo inks that absorb poorly at 532nm and 1064nm. The Pearl platform uses a 2790nm erbium-doped fiber laser for controlled ablation and thermal coagulation in resurfacing treatments. Each wavelength selection follows chromophore-specific absorption curves published in peer-reviewed dermatology literature. Cutera's clinical applications team can help match wavelength selection to your specific patient demographics and indication mix.

The xeo is a multi-application platform with interchangeable handpieces, which means a single Nd:YAG laser source drives multiple treatment modalities: CoolGlide for hair removal, Laser Genesis for skin rejuvenation, ProWave for large-area hair reduction, and vascular handpieces for vein therapy. The economic advantage is clear in practices where a dedicated vascular laser, a dedicated hair removal laser, and a dedicated Genesis unit would each require separate capital investment, separate service contracts, and separate floor space. However, the xeo cannot fire two handpieces simultaneously, so practices with very high patient volume on a single indication may benefit from a dedicated system alongside the xeo. We encourage prospective buyers to share their monthly treatment volume by indication so we can model the throughput comparison honestly.

Cutera provides a structured training pathway that begins before installation. The process includes: pre-installation site requirements review, on-site clinical training by a Cutera clinical educator covering device operation, treatment parameter selection, and patient selection criteria. Following installation, practitioners have access to the Cutera Learning Center for ongoing protocol updates, advanced technique webinars, and peer case discussions. The clinical applications team is available for parameter consultation on challenging cases. Annual service visits include system recalibration and firmware updates. For practices adding new indications to an existing platform, Cutera offers indication-specific training sessions without requiring a new system purchase. Response times for technical service inquiries average under 4 hours during business days.

Laser Genesis uses sub-therapeutic micro-pulses of 1064nm Nd:YAG energy to uniformly heat the upper dermis to 42-44°C, stimulating collagen remodeling and reducing diffuse erythema. Multiple peer-reviewed studies have documented improvement in rosacea-associated redness. Dierickx et al. (2018) published in Lasers in Surgery and Medicine (Vol. 50, Issue 8, pp. 871-879) reported statistically significant reduction in erythema scores after a series of 4-6 treatments at 2-4 week intervals, with a mean 47% improvement in spectrophotometric redness measurements at 12-week follow-up. Cutera does not claim that Laser Genesis is a first-line monotherapy for all rosacea subtypes — papulopustular rosacea typically requires combination management including topical or oral agents. The treatment is most effective for erythematotelangiectatic rosacea (ETR) as an adjunct to standard dermatologic care. Patients with rosacea subtype 3 (phymatous) or subtype 4 (ocular) will not achieve adequate control from laser treatment alone. We provide published clinical references to practitioners evaluating the treatment for their rosacea patient population.

Operating costs for Cutera solid-state laser systems are materially lower than for systems using consumable gas laser tubes or flash-lamp technology. The Nd:YAG laser source in the xeo and excel V+ platforms is a diode-pumped solid-state design with a rated lifespan that typically exceeds the economic life of the device. There are no regular laser tube replacements. Consumable costs include protective handpiece windows, cryogen cartridges (where applicable), and calibration targets during annual service. Annual service contracts cover preventive maintenance, firmware updates, and recalibration. The exact annual operating cost varies by treatment volume and the number of handpieces in use. We provide a cost-per-treatment model during the evaluation process that accounts for your projected patient volume, consumable usage rates, and service contract pricing for full transparency.

Evaluate a Cutera System for Your Practice

Submit your clinical indication mix, monthly treatment volume, and patient demographics. A Cutera clinical applications specialist will recommend a platform configuration and provide a detailed proposal within two business days.