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DEKA Motus PRO

Alexandrite laser (in-motion) · 755 nm alexandrite + 1064 nm Nd:YAG with Moveo and traditional delivery

Technology: Alexandrite Laser

Classification & configurations

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

Motus generations: AX → AY → AZ+ → PRO (current)

Current

At a glance

New price
Not published
FDA status

Record scope: 510(k): K241459 (decision 21 Jun 2024). Checked 4 Sep 2026.

Supplies & recurring costs
Historical Motus-family replacement-part prices are recorded, but exact Motus PRO compatibility, current offers and per-treatment supply costs are not verified.
View supply details
Sources and data on file

Data on file

Recurring consumables
Not verified
FDA
FDA record cited — see scopeK241459
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.

Read FDA-cleared indicationsExact wording from 1 FDA record

K241459 (El.En S.P.A., 2024)

The MOTUS PRO family is a medical device laser family intended for: Alexandrite 755nm laser source: • Temporary hair reduction. • Stable long term or permanent hair reduction through selective targeting of melanin in hair follicles. • 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 on all skin types (Fitzpatrick I-VI) including tanned skin. • Treatment of benign pigmented lesions. • Photocoagulation of benign dermatological vascular lesions (such as port-wine stains, hemangiomas, telangiectasias). Nd:YAG 1064nm laser source: • Removal of unwanted hair, for stable long term or permanent hair reduction and for treatment of PFB. The lasers are indicated on all Skin Types Fitzpatrick I-VI including tanned skin. • Photocoagulation and hemostasis of benign pigmented and benign vascular lesions, such as but not limited to port wine stains, hemangioma, warts, teleangiectasia, rosacea, venous lake, leg veins and spider veins. • Coagulation and hemostasis of soft tissue. • Benign pigmented lesions such as, but not limited to, lentigos, (age spots), solar lentigos (sun spots), café au lait macules, seborrheic keratosis, nevi, cloasma, verrucae, skin tags, keratosis and plaques. • The laser is indicated for benign pigmented lesions to reduce lesion size, for patients with lesions that would potentially benefit from aggressive treatment, and for patients with lesions that have not responded to other laser treatments. • The laser is also indicated for the reduction of red pigmentation in hypertrophic and keloid scars where vascularity is an integral part of the scar. • Treatment of wrinkles.

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

Page updated: October 7, 2026 · How we verify

New-equipment price not yet documented

For a complete budget, ask for an itemized quote covering the device, accessories, training and service.

Price sourcesSources, dates and configurations

No price sources are documented yet. Ask the seller for a current, itemized quote.

Key factsCompany, specifications and verification dates
Key facts
ManufacturerDEKA
CompanyOwner: El.En. Group S.p.A. (Euronext Milan: ELN), ~85% (subsidiary, since 2012) · Distribution: via distributor — Cartessa Aesthetics (exclusive US distributor)
Parent companyEl.En. Group
Brand ownerDEKA
Built by (OEM)DEKA M.E.L.A. S.r.l.
CategoryAlexandrite laser (in-motion)
Technology755 nm alexandrite + 1064 nm Nd:YAG with Moveo and traditional delivery
FDA statusFDA record cited — see scope
510(k) citationK241459
New price rangeNot published
Used price referenceNot published
ConsumablesHistorical Motus-family replacement-part prices are recorded, but exact Motus PRO compatibility, current offers and per-treatment supply costs are not verified.
Launch yearNot published
PricingNot published
Manufacturer-source documents checkedNot published

Overview

Motus PRO is a DEKA laser platform combining 755 nm alexandrite and 1064 nm Nd:YAG sources. The manufacturer lists standard and Moveo handpieces.

The installed handpieces and regional labeling determine the available applications.

Visit product website (cartessaaesthetics.com)

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

510(k): K241459 (decision 21 Jun 2024). Checked 4 Sep 2026.

FDA-cleared indications (verbatim)

K241459 (El.En S.P.A., 2024)

The MOTUS PRO family is a medical device laser family intended for: Alexandrite 755nm laser source: • Temporary hair reduction. • Stable long term or permanent hair reduction through selective targeting of melanin in hair follicles. • 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 on all skin types (Fitzpatrick I-VI) including tanned skin. • Treatment of benign pigmented lesions. • Photocoagulation of benign dermatological vascular lesions (such as port-wine stains, hemangiomas, telangiectasias). Nd:YAG 1064nm laser source: • Removal of unwanted hair, for stable long term or permanent hair reduction and for treatment of PFB. The lasers are indicated on all Skin Types Fitzpatrick I-VI including tanned skin. • Photocoagulation and hemostasis of benign pigmented and benign vascular lesions, such as but not limited to port wine stains, hemangioma, warts, teleangiectasia, rosacea, venous lake, leg veins and spider veins. • Coagulation and hemostasis of soft tissue. • Benign pigmented lesions such as, but not limited to, lentigos, (age spots), solar lentigos (sun spots), café au lait macules, seborrheic keratosis, nevi, cloasma, verrucae, skin tags, keratosis and plaques. • The laser is indicated for benign pigmented lesions to reduce lesion size, for patients with lesions that would potentially benefit from aggressive treatment, and for patients with lesions that have not responded to other laser treatments. • The laser is also indicated for the reduction of red pigmentation in hypertrophic and keloid scars where vascularity is an integral part of the scar. • Treatment of wrinkles.

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

Marketed for

Dual-wavelength laser — 755 nm alexandrite and 1064 nm Nd:YAG with Moveo and traditional delivery

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

Parent company: El.En. Group

Legal manufacturer: DEKA M.E.L.A. S.r.l. (Italy)

Applicant on the FDA record

El.En. S.p.A.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

Supplies & recurring costs

Historical Motus-family replacement-part prices are recorded, but exact Motus PRO compatibility, current offers and per-treatment supply costs are not verified.

·Dealer quote · Updated Aug 30, 2026
Source notes

Historical August 30, 2026 catalog references attributed to LaserXParts and LaserGCC; direct source URLs are not recorded. October 7 editorial correction preserves amounts but flags model-family compatibility, including an explicitly Motus AX rod in a PRO profile.

Parts prices do not establish replacement intervals, per-treatment cost or service contract pricing. Current offers, exact currencies and compatibility remain unverified.

Not yet documented: session schedule, treatment pricing, annual service costs.

Payback calculatorEnter your quote, volume and running costs

Estimate your payback

Enter your quote and treatment costs for DEKA Motus PRO. Published figures appear where available; review them before using the estimate.

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.

New price not published — enter the number on your quote.

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.

Required — include staff time and your own time. Enter 0 only to explicitly exclude labor from this estimate.

Annual service contract ÷ 12, if you carry one.

Your estimate

Enter purchase price, price you charge per treatment, consumable cost per treatment, labor 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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Research comparisons

Includes current and older models.

History8 tracked changes

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

  1. October 7, 2026

    Supply compatibility follow-up 2026-10-07

    Retain historical price amounts while separating model-family replacement parts from recurring treatment supplies. An AX-named rod does not establish PRO compatibility; no new vendor verification or currency conversion claimed.

    Source: https://aestheticindex.co/methodology

  2. October 6, 2026

    DEKA/BTL model documentation and corrections

    Source review on October 6, 2026 of the changed fields only. Prices, lifecycle status and other unchanged fields are not reverified by this update. International brochures do not establish US indications or current service availability.

    Source: https://www.cartessaaesthetics.com/products/motus

  3. October 1, 2026

    Profile overview and accuracy audit

    Added a neutral sourced overview. This is field-specific sourcing, not verification of every other profile field or an endorsement of health-outcome claims.

    Source: https://dekalaser.com/products/motus-pro/

  4. September 4, 2026

    FDA status

    Unknown → Cleared

    Clearance located on openFDA

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

  5. September 4, 2026

    FDA status

    Unknown → Cleared

    Source: Catalog update

  6. September 4, 2026

    510(k) numbers

    K-number set re-verified against openFDA

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

  7. September 4, 2026

    FDA K-numbers

    Source: Catalog update

  8. September 4, 2026

    FDA source URL

    Source: Catalog update

Cite this data: The Aesthetic Index, "DEKA Motus PRO — pricing, FDA status and cost to own", aestheticindex.co (accessed November 3, 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.