Head to head
GentleMax Pro vs Motus PRO (2026)
Compare purchase costs, running costs and the evidence behind each device.
Read the comparison overview
- Purchase cost
- The catalog lists $69,950 (dealer-described unused 2019 unit with three handpieces) for GentleMax Pro. No new-price range is on file for Motus PRO. Check the source notes and request current quotes.
- Technology
- GentleMax Pro: Nd:YAG. Motus PRO: Alexandrite.
- Practice fit
- GentleMax Pro: dual-wavelength platform. Motus PRO: alexandrite laser (in-motion). Check each model’s US regulatory status and labeled indications for your intended use.
Dual-wavelength platform
View full device profile →Alexandrite laser (in-motion)
View full device profile →Price comparison
New price range
- Candela GentleMax Pro
- $69,950 (dealer-described unused 2019 unit with three handpieces)Reported source: Dealer quote · Oct 7, 2026
- DEKA Motus PRO
- Not published
Used price reference
- Candela GentleMax Pro
- 28975-67000 (core cluster 37700-57500)Reported source: Used listing · Aug 30, 2026
- DEKA Motus PRO
- Not published
Payback calculator
- Candela GentleMax Pro
- View ROI calculator
- DEKA Motus PRO
- View cost details
Next step
Explore this model’s specs and owner reviews. For new-equipment inquiries, browse current models.
Browse current modelsSupplies & running costs
Supplies & restrictions
- Candela GentleMax Pro
Read supply costs & requirements
Budget for DCD cryogen and applicable replacement parts. Current US manufacturer prices for cryogen, distance gauges and flashlamps, and cryogen usage for a specified treatment, have not been verified here. The catalog therefore does not establish a per-treatment cost.
Dealer quote · Aug 30, 2026
Supply restrictions: no published lock — no electronic gating documented
View running-cost details- DEKA Motus PRO
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 · Aug 30, 2026
View running-cost details
FDA status & indications
FDA status & indication
- Candela GentleMax Pro
Record scope: Family clearance: K140122 (CANDELA GENTLEMAX FAMILY, Candela Corp., decision 9 May 2014) and K201111 (GentleMax Pro Plus, Candela, decision 26 May 2020, family). Checked 4 Sep 2026.
Read FDA indication wording
“The GentleMAX Family of Laser Systems is indicated for the following at the specified wavelength: 7S5nm Temporary hair reduction. Stable long-term or permanent reduction through selective targeting of melanin in hair follicles. Permanent hair reduction isdefined as long-term stable reduction in the number of hairs regrowing after a treatment regime. 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 [- VI) including tanned skin. Treatment of benign pigmented lesions. Treatment of wrinkles. The photocoagulation of dermatological vascular lesions (such as pant-wine stains, hemangiomas, telangiectasias) 1064nm Removal of unwanted hair, for stable long term or permanent hair reduction and for treatment of PFB. Permanent hair reduction isdefined 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. The lasers are indicated on all skin types Fitzpatrick I-VI including tanned skin. Photocoagulation and hemostasis of pigmented and vascular lesions such as but not limited to port wine stains, hemangioma, warts, telangiectasia, rosacea, venus 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), cafd au ]ait macules, seborrheic keratosis, nevi, chloasma, verrucae, skin tags, keratosis, tattoos (significant reduction in the intensity of black and/or blue-black tattoos) and plaques. The laser is indicated for 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. Reduction of red pigmentation in hypertrophic and keloid scars where vascularity is an integral part of the scar. Treatment of wrinkles. 1064nm Temporary increase of clear nail in patients with onychomycosis (e.g., derniatophytes, Trichophyton rubrum and T. mentagrophytes, and for yeast Candida Albicans, etc.)”
- DEKA Motus PRO
- FDA record cited — see scopeK241459
Record scope: 510(k): K241459 (decision 21 Jun 2024). Checked 4 Sep 2026.
Read FDA indication wording
“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.”
Which chains run each
Chain adoption
- Candela GentleMax Pro
- 3 recorded pairings
- DEKA Motus PRO
- 0 recorded pairings
Chains using it
- Candela GentleMax Pro
- Milan Laser Hair Removal(Confirmed)
- SEV Laser(Confirmed)
- Body Details(Confirmed)
- DEKA Motus PRO
- —
Approved reviews
- Candela GentleMax Pro
- 0
- DEKA Motus PRO
- 0
Specs and platform
Manufacturer
- Candela GentleMax Pro
- Candela
- DEKA Motus PRO
- DEKA
Built by (OEM)
- Candela GentleMax Pro
- Candela Corporation
- DEKA Motus PRO
- DEKA M.E.L.A. S.r.l.
Category
- Candela GentleMax Pro
- Dual-wavelength platform
- DEKA Motus PRO
- Alexandrite laser (in-motion)
Technology
- Candela GentleMax Pro
- 755nm alex + 1064nm Nd:YAG (Nd:YAG)
- DEKA Motus PRO
- 755 nm alexandrite + 1064 nm Nd:YAG with Moveo and traditional delivery (Alexandrite)
Launch year
- Candela GentleMax Pro
- 2013
- DEKA Motus PRO
- —
Status
- Candela GentleMax Pro
- Discontinued
- DEKA Motus PRO
- Current
Manufacturing relationship evidence
- Candela GentleMax Pro
- No separate manufacturing-relationship record linked.
- DEKA Motus PRO
- No separate manufacturing-relationship record linked.
Current alternatives
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