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Lumenis LightSheer Quattro

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Diode laser · 805nm diode, 4 spot sizes

Technology: Diode Laser

Classification & configurations

Category group: Hair removal (diode, alexandrite, Nd:YAG, IPL)

Current

At a glance

New price
$90k–$120kSource not documented
Used asking price
$50k–$75kSource not documented
FDA status
Supplies & recurring costs
HS configurations require a single-use disposable insert between patients (KT-1063750); ET ChillTip runs on gel with no insert.
View supply details
Sources and verified data on file

Data on file

Recurring consumables
Not verified
FDA
FDA ClearedK053628, K170179
Used asking prices
Not verified
  • This panel shows a per-treatment supply cost only when a recorded figure has a dated source.
  • Bottle prices and estimates may still appear under Treatment & running costs.
  • The calculator may include a labeled planning estimate. Review it or enter your own allowance; missing data never means $0.

Figures are reference points, not current offers. Used asking prices are not completed-sale values.

Manufacturer-source documents checked: August 31, 2026

Read FDA-cleared indicationsExact wording from 2 FDA records

K053628 (Lumenis, Inc., 2006)

LightSheer® DuetTM Laser System LightSheer® Pulsed Diode Array Laser Systems are indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer® Pulsed Diode Array Laser Systems are intended for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin. LightSheer® DuetTM Laser Systems with LightSheerV ET T M Laser Handpiece is indicated for the treatment of vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions, and the treatment for pseudofolliculitis barbae. The LightSheer® Dueftm Laser System with LightSheer® ET Tm Laser Handpiece is also indicated for hair removal, permanent hair reduction, and the treatment of benign pigmented lesions and leg veins. LightSheer®DuetTM Laser Systems with LightSheer®HSTh Laser Handpiece is indicated for the treatment of benign vascular and pigmented lesions, hair removal, and permanent hair reduction.

Verbatim from the FDA 510(k) summary, retrieved 8 Sep 2026.

K170179 (Lumenis, Ltd., 2017)

LightSheer Duet: The LightSheer Duet System is indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer Duet System is intended for use on all skin types (Fitzpatrick skin types I – VI), including tanned skin. The LightSheer Duet System with LightSheer ET 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions and leg veins • Treatment of pseudofolliculitis barbae (PFB) • Hair removal, permanent hair reduction* • Treatment of benign pigmented lesions. The LightSheer Duet System with LightSheer HS 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions • Treatment of benign pigmented lesions • Hair removal, and permanent hair reduction*. LightSheer Desire: The LightSheer Desire System is indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer Desire System is intended for use on all skin types (Fitzpatrick skin types I – VI), including tanned skin. The LightSheer Desire System with LightSheer ET/XC 805nm Laser Handpieces are intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions and leg veins • Treatment of pseudofolliculitis barbae (PFB) • Hair removal, permanent hair reduction* • Treatment of benign pigmented lesions. The LightSheer Desire System with LightSheer HS 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions • Treatment of benign pigmented lesions • Hair removal, and permanent hair reduction*. The LightSheer Desire System with LightSheer ET/XC 1060nm and LightSheer HS 1060nm Handpieces are intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia, port wine stains, leg veins and other benign vascular lesions • Hair removal, permanent hair reduction* • Treatment for Pseudofolliculitis Barbae (PFB) • Treatment of benign pigmented lesions, including age spots, solar lentigines, cafe-au-lait spots, nevi of Ota/Ito, melasma, Becker's nevi and other benign pigmented lesions • Treatment of wrinkles

Verbatim from the FDA 510(k) summary, retrieved 8 Sep 2026.

Page updated: September 4, 2026 · How we verify

New and used price references
New$90k–$120k
Source not documented
Used$50k–$75k
Source not documented

Axis runs $0–$120k. Reference figures, not current offers. Used asking prices are not completed-sale values.

Consumable cost per treatment

Not verified

We hold no per-treatment consumable price for this device from a dated source. Ask the seller for a written per-treatment cost.

Price sourcesSources, dates and configurations
New: $90k–$120k·Researched estimate — no dated source on file yet; not a quote.
Used asking range: $50k–$75k·Researched estimate — no dated source on file yet; not a quote.
Key factsCompany, specifications and verification dates
Key facts
ManufacturerLumenis
CompanyOwner: Baring Private Equity Asia (BPEA, now part of EQT) (private equity owned, since 2019) · Distribution: direct
Parent companyLumenis
Brand ownerLumenis
Built by (OEM)Lumenis Be Ltd.
CategoryDiode laser
Technology805nm diode, 4 spot sizes
FDA statusFDA Cleared
510(k) citationK053628, K170179
New price range$90k–$120k
Used asking range$50k–$75k
ConsumablesHS configurations require a single-use disposable insert between patients (KT-1063750); ET ChillTip runs on gel with no insert.
Launch year2019
PricingNot published
Manufacturer-source documents checkedAugust 31, 2026

Overview

Current LightSheer generation

How it worksTechnology and manufacturing

How the technology works

Diode laser with two wavelengths: 805nm (classic LightSheer, strongly absorbed by follicular melanin) and 1060nm (deeper penetrating, less epidermal melanin absorption — safer for Fitzpatrick V-VI and tanned skin). Heats follicle pigment to thermal destruction of the regenerative structures.

Requires pigmented hair — white/gray/true blonde won't respond. Also cleared for benign pigmented/vascular lesions and wrinkles, but bought and used as a hair machine.

Patented technology

The High Speed (HS) vacuum-assist handpiece suctions skin into the 22x35mm aperture, stretching it thin and pulling the follicle closer to the light source — lower fluence, less pain, no gel. ChillTip continuous sapphire cooling on the smaller XC/ET handpieces is genuinely effective epidermal protection.

Origin

Yokneam, Israel (Lumenis Be).

FDA & regulatory detailClearance timeline, authorization route and citation notes
Authorized via 510(k)

Family/platform clearance: K053628 names LightSheer Duet and K170179 names LightSheer Desire/Duet/Infinity; no 510(k) naming LightSheer Quattro was located (checked 4 Sep 2026).

FDA-cleared indications (verbatim)

K053628 (Lumenis, Inc., 2006)

LightSheer® DuetTM Laser System LightSheer® Pulsed Diode Array Laser Systems are indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer® Pulsed Diode Array Laser Systems are intended for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin. LightSheer® DuetTM Laser Systems with LightSheerV ET T M Laser Handpiece is indicated for the treatment of vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions, and the treatment for pseudofolliculitis barbae. The LightSheer® Dueftm Laser System with LightSheer® ET Tm Laser Handpiece is also indicated for hair removal, permanent hair reduction, and the treatment of benign pigmented lesions and leg veins. LightSheer®DuetTM Laser Systems with LightSheer®HSTh Laser Handpiece is indicated for the treatment of benign vascular and pigmented lesions, hair removal, and permanent hair reduction.

Verbatim from the FDA 510(k) summary, retrieved 8 Sep 2026.

K170179 (Lumenis, Ltd., 2017)

LightSheer Duet: The LightSheer Duet System is indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer Duet System is intended for use on all skin types (Fitzpatrick skin types I – VI), including tanned skin. The LightSheer Duet System with LightSheer ET 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions and leg veins • Treatment of pseudofolliculitis barbae (PFB) • Hair removal, permanent hair reduction* • Treatment of benign pigmented lesions. The LightSheer Duet System with LightSheer HS 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions • Treatment of benign pigmented lesions • Hair removal, and permanent hair reduction*. LightSheer Desire: The LightSheer Desire System is indicated for use in surgical, aesthetic, and cosmetic applications in the medical specialties of general and plastic surgery, and dermatology. The LightSheer Desire System is intended for use on all skin types (Fitzpatrick skin types I – VI), including tanned skin. The LightSheer Desire System with LightSheer ET/XC 805nm Laser Handpieces are intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions and leg veins • Treatment of pseudofolliculitis barbae (PFB) • Hair removal, permanent hair reduction* • Treatment of benign pigmented lesions. The LightSheer Desire System with LightSheer HS 805nm Laser Handpiece is intended for: • Treatment of benign vascular lesions • Treatment of benign pigmented lesions • Hair removal, and permanent hair reduction*. The LightSheer Desire System with LightSheer ET/XC 1060nm and LightSheer HS 1060nm Handpieces are intended for: • Treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia, port wine stains, leg veins and other benign vascular lesions • Hair removal, permanent hair reduction* • Treatment for Pseudofolliculitis Barbae (PFB) • Treatment of benign pigmented lesions, including age spots, solar lentigines, cafe-au-lait spots, nevi of Ota/Ito, melasma, Becker's nevi and other benign pigmented lesions • Treatment of wrinkles

Verbatim from the FDA 510(k) summary, retrieved 8 Sep 2026.

Marketed for

Diode laser — 805nm diode, 4 spot sizes

Marketing claims are the manufacturer's own and are not the same as a cleared indication.

Parent company: Lumenis

Legal manufacturer: Lumenis Be Ltd. (Israel)

Applicant on the FDA record

Lumenis Be Ltd.The applicant named on the FDA record can differ from the brand shown on the device.

Regulatory data comes from public FDA records and may lag recent updates. Confirm the applicable status and documentation before purchase.

Treatment & running costs

Treatments

Sessions & timing

No treatment schedule documented yet.

What practices charge

No sourced treatment price on file.

Supplies & recurring costs

HS configurations require a single-use disposable insert between patients (KT-1063750); ET ChillTip runs on gel with no insert.

·Dealer quote · Updated Aug 31, 2026
Source notes

Single-use HS insert requirement from Lumenis in-service (part KT-1063750). Pack pricing is a secondary-market asking price (single-unit listings, Aug 2026), not OEM list.

Annual service & support

No annual service cost documented yet.

Payback calculatorModel your own volume, labor and service costs

Estimate your payback

Pre-filled from our published Lumenis LightSheer Quattro data where we have it. Estimates appear once the required inputs are available. Review and adjust every pre-filled value before relying on the result.

Start from

No verified per-treatment supply cost is on file. Enter your own allowance. Use $0 only if you have confirmed that it applies to your practice.

Pre-filled from the midpoint of the published new-price range

20 is an illustrative default — change it to your volume.

No sourced per-session price on file — enter what you charge.

Required — enter your cost; missing data does not mean $0.

Provider or tech time for one treatment, fully loaded. Enter 0 if you own-operate.

Annual service contract ÷ 12, if you carry one.

Your estimate

Enter price you charge per treatment, consumable cost per treatment to see contribution and a payback range.

This model ignores financing — if you lease or borrow, add your monthly payment. Estimates from your inputs and our published ranges — not a projection, guarantee or financial advice. How we calculate this.

ComplianceScreening and contraindications on the manufacturer's record

Contraindications & screening

Recent tanning/self-tanner, isotretinoin washout (commonly 6 months), pregnancy, active infection/herpes in the area, photosensitizers, keloid history, gold therapy. Gray/white/blonde hair is a futility screen — don't sell those patients packages.

Warranty & serviceWhat to confirm in writing before you buy

Before buying new or used, confirm in writing:

  • Current warranty coverage
  • Included training
  • Service terms

Chains using this device

A chain listing does not establish availability at every location.

No confirmed chain deployments recorded yet.

Owner & operator reviews

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Current alternatives

Current catalog models to research. Confirm availability and configuration with the supplier.

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History4 tracked changes

Every tracked change to pricing, lifecycle status, FDA data and warranty terms — newest first.

  1. September 4, 2026

    FDA K-numbers

    Source: Catalog update

  2. September 4, 2026

    FDA source URL

    Source: Catalog update

  3. September 4, 2026

    510(k) numbers

    K-number set re-verified against openFDA

    Source: Council round 2 audit, verified on openFDA 2026-09-04

  4. August 1, 2026

    Record created

    Added to The Aesthetic Index — August 2026

    Source: The Aesthetic Index editorial

Cite this data: The Aesthetic Index, "Lumenis LightSheer Quattro — pricing, FDA status and cost to own", aestheticindex.co (accessed September 24, 2026).

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Device and company names are trademarks of their respective owners. The Aesthetic Index is not affiliated with or endorsed by any manufacturer, distributor or lender named here, except as disclosed. Price figures are references, not current offers. Check each device’s source notes. Not medical, legal or regulatory advice.