Lumenis LightSheer Desire
Diode laser · 805nm diode, 3 handpieces
Technology: Diode Laser
Classification & configurations
Category group: Hair removal (diode, alexandrite, Nd:YAG, IPL)
At a glance
- New-unit reference · older model
- Not published
- Used asking price
- $25k–$45kSource not documented
- FDA status
- Supplies & recurring costs
- Supply details not yet documented.
Sources and verified data on file
Data on file
- Recurring consumables
- Not verified
- Used asking prices
- Not verified
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Figures are reference points, not current offers. Used asking prices are not completed-sale values.
Read FDA-cleared indicationsExact wording from 2 FDA records
K151947 (Lumenis, Ltd., 2015)
The 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. The LightSheer Desire Light Laser System with LightSheer ET/XC Laser Handpiece is indicated for the treatment of vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions, the treatment of Pseudofolliculitis Barbae (PFB). The LightSheer Desire Light Laser System with LightSheer ET/XC Laser Handpiece is also indicated for hair removal, permanent hair reduction* and the treatment of benign pigmented lesions and leg veins. * Note: Permanent hair reduction is defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime. Modified Device Description: The modified LightSheer Desire Light Laser System is a non-invasive aesthetic laser system that delivers pulsed infrared laser light with a wavelength ranging from 790-830 nm (805 nm nominal). The system consists of a laser console and two optional handpieces, ET or XC, which can be connected to the console, one at a time, via a universal plug-in connector and an umbilical cable. The ET handpiece; delivers laser energy through a 9mm x 9mm tip up to 81 J maximum.
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: August 6, 2026 · How we verify
No new-unit price reference is published for this older model.
Axis runs $0–$45k. Reference figures, not current offers. Used asking prices are not completed-sale values.
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
Key factsCompany, specifications and verification dates
| Manufacturer | Lumenis |
|---|---|
| Company | Owner: Baring Private Equity Asia (BPEA, now part of EQT) (private equity owned, since 2019) · Distribution: direct |
| Parent company | Lumenis |
| Brand owner | Lumenis |
| Built by (OEM) | Lumenis Be Ltd. |
| Category | Diode laser |
| Technology | 805nm diode, 3 handpieces |
| FDA status | FDA Cleared |
| 510(k) citation | K151947, K170179 |
| New-unit reference (older model) | Not published |
| Used asking range | $25k–$45k |
| Consumables | Not published |
| Launch year | 2014 |
| Pricing | Not published |
| Manufacturer-source documents checked | Not published |
Overview
Refined Duet successor
FDA & regulatory detailClearance timeline, authorization route and citation notes
FDA-cleared indications (verbatim)
K151947 (Lumenis, Ltd., 2015)
The 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. The LightSheer Desire Light Laser System with LightSheer ET/XC Laser Handpiece is indicated for the treatment of vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions, the treatment of Pseudofolliculitis Barbae (PFB). The LightSheer Desire Light Laser System with LightSheer ET/XC Laser Handpiece is also indicated for hair removal, permanent hair reduction* and the treatment of benign pigmented lesions and leg veins. * Note: Permanent hair reduction is defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime. Modified Device Description: The modified LightSheer Desire Light Laser System is a non-invasive aesthetic laser system that delivers pulsed infrared laser light with a wavelength ranging from 790-830 nm (805 nm nominal). The system consists of a laser console and two optional handpieces, ET or XC, which can be connected to the console, one at a time, via a universal plug-in connector and an umbilical cable. The ET handpiece; delivers laser energy through a 9mm x 9mm tip up to 81 J maximum.
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, 3 handpieces
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, 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
Consumable costs are not documented yet.
Annual service & support
No annual service cost documented yet.
Payback calculatorModel your own volume, labor and service costs
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History1 tracked change
Every tracked change to pricing, lifecycle status, FDA data and warranty terms — newest first.
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 Desire — pricing, FDA status and cost to own", aestheticindex.co (accessed September 24, 2026).
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