Lumenis LightSheer Infinity
Diode laser · 805nm diode, vacuum + ChillTip
Technology: Diode Laser
Classification & configurations
Category group: Hair removal (diode, alexandrite, Nd:YAG, IPL)
At a glance
- New price
- $100k–$130kSource 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
- FDA
- FDA ClearedK170179
- 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.
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Figures are reference points, not current offers.
Read FDA-cleared indicationsExact wording from 1 FDA record
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
Axis runs $0–$130k. Reference figures, not current offers.
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, vacuum + ChillTip |
| FDA status | FDA Cleared |
| 510(k) citation | K170179 |
| New price range | $100k–$130k |
| Used asking range | Not published |
| Consumables | Not published |
| Launch year | 2022 |
| Pricing | Not published |
| Manufacturer-source documents checked | Not published |
Overview
Newest LightSheer tier above Quattro
FDA & regulatory detailClearance timeline, authorization route and citation notes
510(k): K170179. Checked 4 Sep 2026.
FDA-cleared indications (verbatim)
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, vacuum + ChillTip
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
Consumable costs are not documented yet.
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 Infinity 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.
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Your estimate
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Warranty & serviceWhat to confirm in writing before you buy
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- Current warranty coverage
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History6 tracked changes
Every tracked change to pricing, lifecycle status, FDA data and warranty terms — newest first.
September 4, 2026
FDA status
Unknown → Cleared
Clearance located on openFDA
Source: Council round 2 audit, verified on openFDA 2026-09-04
September 4, 2026
FDA status
Unknown → Cleared
Source: Catalog update
September 4, 2026
510(k) numbers
K-number set re-verified against openFDA
Source: Council round 2 audit, verified on openFDA 2026-09-04
September 4, 2026
FDA K-numbers
Source: Catalog update
September 4, 2026
FDA source URL
Source: Catalog update
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 Infinity — pricing, FDA status and cost to own", aestheticindex.co (accessed September 24, 2026).
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