Submental aesthetics · 520 nm green + 405 nm violet

CLX Laser

A precise, non-thermal approach to the under-chin area

Overview

About the CLX Laser

CLX pairs 520 nm green and 405 nm violet wavelengths in a touchless, non-thermal platform for non-invasive aesthetic treatment to improve the appearance of the submental (under-chin) area. Treatment is delivered without contact or therapeutic heating, with 15-minute sessions and no procedural downtime.

  • 520 nm green and 405 nm violet wavelengths
  • Touchless, non-thermal treatment
  • Eight 15-minute sessions over four weeks
  • No needles, incisions or per-session consumables

Typical applications

  • Non-invasive aesthetic improvement of the submental (under-chin) area
  • Aesthetic practices and medically supervised facial aesthetics
  • A focused addition to a body-contouring clinic's services
CLX Laser laser device

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Product description

What the device does

CLX is a focused aesthetic platform for the submental area. Patients rest comfortably while the device operates, without needles, incisions, anaesthesia or therapeutic heating. Erchonia describes the protocol as eight 15-minute, non-contact sessions delivered over four weeks.

The hands-free approach offers a streamlined service for aesthetic practices, facial aesthetics and body-contouring clinics. There are no applicator cards, gels, syringes or consumable kits to restock for each session.

Unlike a full-body circumference-reduction platform, CLX is focused on improving the appearance of the under-chin area. Suitability and treatment planning should be assessed by a medical professional.

Erchonia CLX green and violet laser unit

Mechanism

How it works

CLX delivers specific green and violet wavelengths through a non-contact, non-thermal approach. Erchonia describes the technology in terms of the energy carried by each photon and the biological response to an appropriate light dose, rather than wattage and heat.

In the clinical study, the mechanism is described as stimulating adipocytes to release stored lipid content without destroying the cells. Released lipids are processed naturally by the body, with the appearance of the submental area changing over the treatment course.

Patients rest during each 15-minute session and can return to their day without procedural downtime. Individual results vary.

FDA indications for use

Clearance K252574

  • a.Non-invasive aesthetic treatment to improve the appearance of the submental (under-chin) area.

Device intended for medical professionals. Prescription use (21 CFR 801 Subpart D). Individual results may vary.

Specifications

At a glance

Wavelengths

520 nm green & 405 nm violet

Treatment area

Submental (under-chin) area

Delivery

Non-contact, hands-free

Thermal profile

Non-thermal; no therapeutic heating

Session length

15 minutes

Study protocol

8 sessions over 4 weeks

Procedural downtime

None

Per-session consumables

No applicator cards, gels or consumable kits

Use

Prescription use; medical professionals

Clinical evidence

Eight sessions. Blinded review.

Erchonia reports a prospective, dual-centre study in adults with measurable submental fat. Participants received eight 15-minute treatments over four weeks. Three independent, board-certified cosmetic surgeons assessed photographs in a blinded review.

86.7%
Blinded-review success on an intent-to-treat basis — and 95.8% correct identification of the post-treatment photograph at the 12-week follow-up.

Intent-to-treat: 86.7%; per-protocol at 12 weeks: 95.8%. Erchonia CLX dual-centre clinical study.

5.45 mm
Mean reduction in submental skinfold thickness, with BMI stable — the change is under the chin, not on the scale.

Erchonia CLX dual-centre clinical study. Individual results vary.

92%
Patient satisfaction at 12 weeks, with zero device-related adverse events.

Erchonia CLX dual-centre clinical study.

CLX study participant one: side and front views of the under-chin area before and after treatment
Submental · before and after
CLX study participant two: side and front views of the under-chin area before and after treatment
Submental · before and after
CLX study participant three: side and front views of the under-chin area before and after treatment
Submental · before and after

Manufacturer-reported study outcomes, not guaranteed results. Individual results vary. US FDA clearance does not establish Australian regulatory status.

Read Erchonia’s CLX clinical study summary

Compare

How to choose the right device for your clinic

Every laser in the Erchonia portfolio is a valuable addition. This matrix compares format, wavelength and FDA-cleared indication across the range.

Comparison of the Erchonia laser range by wavelength, format and FDA-cleared indication
Choosing the right device
CLX Laser deviceCLX Laser520 nm green + 405 nm violet
Emerald Laser deviceEmerald Laser10 × 520–542 nm green
GVL Laser deviceGVL Laser520 nm green + 405 nm violet
EVRL Laser deviceEVRL Laser640 nm red + 405 nm violet
FX 405 Laser deviceFX 405 Laser640 nm red + 405 nm violet
Lunula Laser deviceLunula Laser640 nm red + 405 nm violet
Collimated, monochromatic, coherent true laserYesYesYesYesYesYes
Non-thermal — no heat, pain or downtimeYesYesYesYesYesYes
Short 10–30 minute treatmentsYesYesYesYesYesYes
Handheld and portableNot specifiedNoYesYesNoNo
Automated — hands-free during treatmentYesYesNoNoYesYes
Green wavelength (520–542 nm)YesYesYesNoNoNo
Red wavelength (640 nm)NoNoNoYesYesYes
Violet wavelength (405 nm)YesNoYesYesYesYes
Musculoskeletal pain indicationNoNoYesYesYesNo
Dermatological / acne indicationNoNoYesYesNoNo
Body circumference reduction indicationNoYesNoNoNoNo
Onychomycosis (clear nail growth) indicationNoNoNoNoNoYes
Post-operative pain indicationNoNoNoNoYesNo
FDA market cleared, ISO/IEC compliantNot specifiedYesYesYesYesYes
Submental (under-chin) aesthetic indicationYesNoNoNoNoNo

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