CE Marked medical device conforming to applicable European and UK medical device directives/regulations for laser systems.
Class 4/Class IV laser system, requiring compliance with relevant laser safety standards and local regulatory requirements.
Manufactured under Lumenis quality management systems aligned with international standards for medical devices (e.g., ISO 13485).
CE Marked medical device conforming to applicable European and UK medical device directives/regulations for laser systems.
Class 4/Class IV laser system, requiring compliance with relevant laser safety standards and local regulatory requirements.
Manufactured under Lumenis quality management systems aligned with international standards for medical devices (e.g., ISO 13485).
Subject to FDA 510(k) clearance for hair removal, permanent hair reduction, PFB, benign pigmented lesions and benign vascular lesions in applicable markets; local indications may vary by region.
Description
The Lumenis LightSheer DESIRE is a diode laser platform designed primarily for long-term hair reduction and the treatment of benign vascular and pigmented lesions. It uses the industry-standard 805 nm diode wavelength and, in some configurations, also supports a 1060 nm wavelength. The system incorporates two advanced technologies: High-Speed vacuum-assisted technology (HS) for large areas and ChillTip integrated contact cooling (XC and ET handpieces) for precise, high-fluence treatments. Equipped with up to three interchangeable handpieces (HS 22 × 35 mm, XC 12 × 12 mm and ET 9 × 9 mm), the LightSheer DESIRE can effectively treat all body areas with tailored spot sizes and fluence levels. The unit described in this listing is a used system, approximately 7.5 years old, which has been serviced annually from new and was most recently serviced at the end of May 2025.
Bnefits
Versatile 805 nm diode laser (with optional 1060 nm capability in some configurations) suitable for hair removal and a range of aesthetic indications.
Three interchangeable handpieces (HS, XC, ET) with different spot sizes to treat all body areas efficiently and comfortably.
High-Speed HS handpiece (22 × 35 mm) with vacuum-assisted technology for rapid, low-fluence treatment of large body areas without gel.
XC and ET handpieces with Sapphire ChillTip contact cooling for epidermal protection and comfortable treatment of small and medium areas at higher fluence.
Clinically established for permanent hair reduction, including treatment of Pseudofolliculitis Barbae (PFB), with long-lasting results.
Multi-application capability for benign vascular lesions (e.g., angiomas, hemangiomas, telangiectasia, leg veins) and benign pigmented lesions.
Intuitive graphical user interface with presets for various skin types and treatment areas, supporting consistent outcomes and easier delegation.
Upgradeable and scalable platform, allowing additional handpieces or capabilities to be added as a clinic grows.
Used system in this listing has documented annual servicing from new, with last service performed at the end of May 2025.
Indications
Hair removal and permanent hair reduction for unwanted hair on the face and body across all Fitzpatrick skin types (I–VI), including tanned skin.
Subject to FDA 510(k) clearance for hair removal, permanent hair reduction, PFB, benign pigmented lesions and benign vascular lesions in applicable markets; local indications may vary by region.
Diode laser hair removal system
Treatment of Pseudofolliculitis Barbae (PFB), commonly known as razor bumps.
Treatment of benign vascular lesions including angiomas, hemangiomas, telangiectasia, leg veins and other benign vascular lesions.
Treatment of benign pigmented lesions such as solar lentigines and other superficial cosmetic pigmented lesions.
In some regulatory jurisdictions and configurations, treatment of leg veins and selected wrinkles, according to the device’s clearances and local regulations.
Composition
Laser type: high-power diode laser system.
Primary wavelength: 805 nm diode; some DESIRE configurations support dual wavelengths (805 nm and 1060 nm) for customised treatments.
Handpieces: HS (High-Speed vacuum-assisted handpiece, 22 × 35 mm spot size), XC (ChillTip handpiece, 12 × 12 mm spot size) and ET (ChillTip handpiece, 9 × 9 mm spot size).
Fluence range: up to approximately 100 J/cm² (depending on handpiece and pulse width).
Pulse duration: variable; typical range approximately 5–400 ms.
Comfort and safety technologies: Vacuum Assisted High-Speed Integrated Technology (HS) and ChillTip Sapphire contact cooling (XC and ET).
Console: touch-screen control unit with integrated power supply, cooling, electronics and safety interlocks.
Accessories: operator and patient laser safety eyewear, footswitch, power cables and user manuals (exact included accessories may vary by reseller and configuration of this used system).
Formulation
Compact, portable laser workstation designed for use in aesthetic and dermatology clinics.
Three easily interchangeable handpieces to tailor spot size and technology (vacuum assist or ChillTip cooling) to treatment area and indication.
Advanced software with preset and customisable treatment parameters based on body area, skin type, hair colour and thickness.
Integrated contact cooling in ChillTip handpieces for continuous epidermal protection before, during and after laser pulse delivery.
Vacuum-assisted technology in the HS handpiece draws the skin into the handpiece, stretches it and brings follicles closer to the energy source, enabling lower fluence and improved comfort.
Laser classification: Class 4 / Class IV therapeutic laser system, requiring appropriate safety measures and protective eyewear.
Packaging
Capital equipment system typically comprising the LightSheer DESIRE console, one or more handpieces (HS, XC, ET), footswitch, safety eyewear and manuals.
Supplied on a mobile cart or with integrated wheels for easy positioning within the treatment room.
When sold as a used system, the configuration and included accessories (e.g., number and type of handpieces, eyewear, manuals) depend on the original owner and reseller; buyers should confirm exact contents with the seller.
Shipped in protective crate or original-equivalent packaging for transport, with shock and tilt indicators recommended for safe delivery.
Usage
For professional use only by trained physicians or licensed aesthetic practitioners operating under applicable local regulations.
Perform a full consultation including medical history, medications, skin type assessment, hair characteristics and evaluation of contraindications before treatment.
Prepare the treatment area by shaving hair if necessary, cleansing the skin and removing make-up, lotions, deodorants and self-tanning products.
Select the appropriate handpiece (HS for large areas, XC or ET for small or detail work) and choose initial treatment parameters based on skin type, hair thickness and body area using the system presets as a guide.
Ensure all staff and the patient wear wavelength-appropriate laser safety eyewear and that a laser-controlled area is established according to local laser safety policies.
Place the handpiece perpendicular to the skin with adequate contact or vacuum engagement, and deliver pulses according to the recommended pattern, maintaining slight overlap where indicated.
Monitor clinical endpoints such as perifollicular erythema and oedema while avoiding excessive whitening, blistering or patient discomfort; adjust fluence, pulse width or cooling as needed.
Provide aftercare instructions, including avoiding sun exposure and tanning, using broad-spectrum SPF, and monitoring for transient redness or swelling.
Schedule follow-up sessions at intervals appropriate to the body area and hair growth cycle (often 4–8 weeks apart) until satisfactory hair reduction is achieved.
For this used system, adhere carefully to any additional maintenance and calibration recommendations provided in the service records and by Lumenis or authorised service providers.
Contraindications
Active infection, inflammation, open wounds or compromised skin integrity in the proposed treatment area.
Known photosensitive disorders or concurrent use of photosensitising medications at risk for adverse reactions to 805/1060 nm light.
Recent significant sun exposure, sunburn or use of tanning beds/self-tanning products on the treatment area.
History of keloid formation or hypertrophic scarring in the intended treatment zone, unless carefully evaluated and cleared by a specialist.
Pregnancy or breastfeeding, as laser hair removal in these populations is typically avoided due to limited safety data in aesthetic indications.
Presence of suspicious pigmented lesions or active skin malignancy in the treatment area.
Patients with unrealistic expectations or underlying endocrine conditions affecting hair growth who are not under appropriate medical care.
Inability or unwillingness to comply with pre- and post-treatment care requirements, including sun avoidance and skin care instructions.
Adverse Effects
Common, transient effects such as erythema, perifollicular oedema, warmth, mild discomfort or a sunburn-like sensation at the treated site.
Temporary changes in skin pigmentation, including hyperpigmentation or hypopigmentation, particularly in darker or recently tanned skin.
Blistering, crusting or superficial burns if excessive fluence is used or if cooling/contact is inadequate.
Rare risk of scarring or long-lasting textural changes in cases of significant thermal injury.
Paradoxical hypertrichosis (increased hair growth) in rare cases, particularly in areas with fine vellus hair.
Potential ocular injury if appropriate eye protection is not used; strict adherence to laser safety protocols is essential.
Allergic or irritant reactions to any topical products used before or after treatment rather than to the laser itself.
Storage Conditions
Install and store the system in a clean, dry, well-ventilated clinical environment with stable ambient temperature and humidity within the range specified in the operator manual.
Keep the device away from direct sunlight, moisture and extreme temperatures, and ensure that cooling vents and air inlets are unobstructed.
Place the system on a stable, level surface or use the integrated wheels on a suitable floor to prevent tipping or movement during operation.
Disconnect the system from mains power before cleaning, relocating or performing maintenance as recommended by the manufacturer or authorised service provider.
For this used system, maintain the service schedule as advised in the original documentation, with periodic servicing by an authorised engineer to ensure ongoing safety and performance.
Duration
Hair reduction treatment typically involves a series of multiple sessions (often around 4\u20138 or more), spaced approximately 4\u20138 weeks apart depending on the body area and hair growth cycle. Each session for a large area (e.g., legs or back) can usually be completed within 15\u201360 minutes, depending on handpiece choice and clinic protocol.
Onset
Early results, such as shedding of treated hairs and visible reduction in hair growth, are generally observed within several days to a few weeks after each session. Progressive long-term hair reduction develops over the full course of treatment, with durable outcomes evaluated at 6, 9 and 12 months after completion of a treatment series.
