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Lumenis Legend Pro

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Combination Face Platform · TriPollar RF + DMA + Voluderm

Classification & configurations

Category group: Skin tightening & remodeling (RF microneedling, monopolar RF, HIFU)

Legacy model

At a glance

New-unit reference · older model
Not published
Used asking price
$15k–$28kSource not documented
FDA status
Supplies & recurring costs
Supply details not yet documented.
View supply details
Sources and verified data on file

Data on file

Recurring consumables
Not verified
FDA
FDA ClearedK171359, K173503, K200545
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.

Read FDA-cleared indicationsExact wording from 3 FDA records

K171359 (Pollogen, Ltd., 2017)

The Pollogen Legend+™ System is intended for dermatological procedures requiring ablation and resurfacing of the skin when using VoluDerm Energy (Applicator VO). It is also intended for use in dermatologic and general surgical procedures for the non-invasive treatment of mild to moderate facial wrinkles and rhytides when using TriPollar RF Energy (Applicators 1-3).

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

K173503 (Pollogen, Ltd., 2018)

The Modified Legend+™ system is intended for dermatological procedures requiring ablation and resurfacing of the skin when using VoluDerm Energy (Applicator VO). It is also intended for use in dermatologic and general surgical procedures for the non-invasive treatment of mild to moderate facial wrinkles and rhytides when using TriPollar RF Energy (Applicators 1-3). Modified Device Description Pollogen Ltd’s modified Legend+™system delivers bipolar radiofrequency (RF) electrical current to the skin surface for dermatological procedures requiring ablation and resurfacing of the skin. The physician can control the parameters of the device through a user interface. The system consists of: - Main Unit (includes the Controller); - Control Panel (User Interface); - RF Generator; - VO (VoluDerm) Treatment Applicator - Disposable tips; gen12, gen36 & gen36L - Treatment Applicators 1-3 (TriPollar); - Foot Switch; - Patient-Controlled Manual Switch. The device generates RF energy, which is applied to the skin. The VO (VoluDerm Energy) treatment applicator applies pulses of bipolar RF energy that flows between electrodes to create micro-ablation points on the skin via an array of multi-electrode pins. The TriPollar treatment Applicators 1-3 apply bipolar RF energy that flows between electrodes on the skin. The three applicators differ in size and configuration and are indicated for treatment of various size facial areas. The operator can adjust treatment parameters, such as the power level and treatment time from the user interface on the Main Unit. The Applicator is applied with a little pressure and a rubbing/massaging technique (linear, circular, etc., depending on the area). The applicator should be moved continuously on the skin. No active cooling of the electrodes or the skin is required.

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

K200545 (Pollogen, Ltd., 2021)

Legend Pro DMA is intended for muscle conditioning to stimulate healthy muscles. Legend Pro DMA is not intended to be used in conjunction with therapy or treatment of medical diseases or medical conditions of any kind. Legend Pro DMA is intended to be operated by a trained professional who is present to monitor treatment.

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.

Used asking price reference
Used$15k–$28k
Source not documented

Axis runs $0–$28k. 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
Used asking range: $15k–$28k·Researched estimate — no dated source on file yet; not a quote.
Key factsCompany, specifications and verification dates
Key facts
ManufacturerLumenis (Pollogen)
CompanyOwner: Baring Private Equity Asia (BPEA, now part of EQT) (private equity owned, since 2019) · Distribution: direct
Parent companyLumenis
Brand ownerLumenis
Built by (OEM)Pollogen Ltd.
CategoryCombination Face Platform
TechnologyTriPollar RF + DMA + Voluderm
FDA statusFDA Cleared
510(k) citationK171359, K173503, K200545
New-unit reference (older model)Not published
Used asking range$15k–$28k
ConsumablesNot published
Launch year2018
PricingNot published
Manufacturer-source documents checkedNot published

Overview

Predecessor to Legend Pro+

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

FDA-cleared indications (verbatim)

K171359 (Pollogen, Ltd., 2017)

The Pollogen Legend+™ System is intended for dermatological procedures requiring ablation and resurfacing of the skin when using VoluDerm Energy (Applicator VO). It is also intended for use in dermatologic and general surgical procedures for the non-invasive treatment of mild to moderate facial wrinkles and rhytides when using TriPollar RF Energy (Applicators 1-3).

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

K173503 (Pollogen, Ltd., 2018)

The Modified Legend+™ system is intended for dermatological procedures requiring ablation and resurfacing of the skin when using VoluDerm Energy (Applicator VO). It is also intended for use in dermatologic and general surgical procedures for the non-invasive treatment of mild to moderate facial wrinkles and rhytides when using TriPollar RF Energy (Applicators 1-3). Modified Device Description Pollogen Ltd’s modified Legend+™system delivers bipolar radiofrequency (RF) electrical current to the skin surface for dermatological procedures requiring ablation and resurfacing of the skin. The physician can control the parameters of the device through a user interface. The system consists of: - Main Unit (includes the Controller); - Control Panel (User Interface); - RF Generator; - VO (VoluDerm) Treatment Applicator - Disposable tips; gen12, gen36 & gen36L - Treatment Applicators 1-3 (TriPollar); - Foot Switch; - Patient-Controlled Manual Switch. The device generates RF energy, which is applied to the skin. The VO (VoluDerm Energy) treatment applicator applies pulses of bipolar RF energy that flows between electrodes to create micro-ablation points on the skin via an array of multi-electrode pins. The TriPollar treatment Applicators 1-3 apply bipolar RF energy that flows between electrodes on the skin. The three applicators differ in size and configuration and are indicated for treatment of various size facial areas. The operator can adjust treatment parameters, such as the power level and treatment time from the user interface on the Main Unit. The Applicator is applied with a little pressure and a rubbing/massaging technique (linear, circular, etc., depending on the area). The applicator should be moved continuously on the skin. No active cooling of the electrodes or the skin is required.

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

K200545 (Pollogen, Ltd., 2021)

Legend Pro DMA is intended for muscle conditioning to stimulate healthy muscles. Legend Pro DMA is not intended to be used in conjunction with therapy or treatment of medical diseases or medical conditions of any kind. Legend Pro DMA is intended to be operated by a trained professional who is present to monitor treatment.

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

Marketed for

Combination Face Platform — TriPollar RF + DMA + Voluderm

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

510(k) numbers

K171359, K173503, K200545

Parent company: Lumenis

Legal manufacturer: Pollogen Ltd. (Israel)

Applicant on the FDA record

Pollogen, 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 Legend Pro 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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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.

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

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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.

Warranty & serviceWhat to confirm in writing before you buy

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  • Current warranty coverage
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Current alternatives

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History1 tracked change

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

  1. August 1, 2026

    Record created

    Added to The Aesthetic Index — August 2026

    Source: The Aesthetic Index editorial

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

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