Technology
Every device chosen for its evidence.
Our clinic is equipped with a carefully curated portfolio of best-in-class, clinically proven technologies — each selected for its safety profile and its ability to work as part of a broader, personalised treatment strategy.
Overview
“Technology, selected with purpose.”
EVE MUSE
Advanced imaging and AI-powered analysis designed to assess skin condition, facial structure and key visual markers beneath the surface. EVE MUSE provides objective data to support more precise consultations, personalised treatment planning and consistent tracking of results over time.
XERF
Multifrequency monopolar radiofrequency combining 6.78 MHz and 2 MHz to tighten at more than one tissue depth.
Ultherapy PRIME
Microfocused ultrasound with real-time imaging, precisely targeted to the tissue depth involved in skin lifting.
UltraClear
Powered by 2910 nm cold fibre laser technology, delivering precise, controlled fractional ablation with minimal excess heat — from a subtle skin refresh to more intensive resurfacing.
CUTERA Pico enlighten
Picosecond and nanosecond pulses across multiple wavelengths, targeting pigment at different depths with limited thermal impact.
Excel V+
A dual-wavelength 532 nm KTP and 1064 nm Nd:YAG platform for redness, vascular lesions, acne and selected pigmentation.
Laser Genesis
Gentle, non-ablative rejuvenation using 532 nm and 1064 nm wavelengths for redness, tone, texture and collagen stimulation.
EMTONE
Monopolar radiofrequency combined with targeted acoustic shockwave energy to address cellulite and improve skin firmness.Monopolar radiofrequency and Targeted Pressure Energy delivered simultaneously to address cellulite and skin firmness.
Dermalux Tri-Wave MD
Three clinically established wavelengths of LED light, used alone or in combination, to support cellular repair, skin recovery and rejuvenation with no downtime.
Hydrafacial
Cleansing, exfoliation, extraction and hydration in one — the maintenance ritual between clinical treatments.
Advanced AI Skin & Facial Analysis
EVE MUSE
Why we chose it
We selected EVE MUSE to bring greater objectivity and precision to the consultation process. Advanced imaging and AI analysis allow us to visualise and monitor skin characteristics that may not be apparent to the naked eye, supporting a more personalised approach to treatment planning.
Technology differentiation
EVE MUSE combines high-resolution 3D imaging, multispectral photography and AI-powered analysis. Multiple cameras and specialised lighting capture detailed images of the face from different angles, providing a comprehensive assessment of the skin and facial structure.
What we assess
The system evaluates 40+ skin and ageing indicators, including pigmentation, wrinkles, pores, redness and other skin characteristics, alongside facial proportions, contours and volume. Results can be recorded and compared over time to objectively monitor changes following treatment or skincare.
Clinical value
EVE MUSE provides a standardised visual baseline before treatment, helping us identify individual priorities and develop a more tailored treatment plan. Repeat imaging allows changes to be documented objectively, supporting a measured and evidence-led approach to aesthetic care.
Sessions & Recovery
EVE MUSE analysis is non-invasive, contact-free and requires no preparation or downtime. The imaging process takes only a few moments and the results can be reviewed during your consultation.
Please note: EVE MUSE is an imaging and analysis tool. Its results are intended to support consultation and treatment planning and do not replace a clinical assessment or medical diagnosis.
Precision Ultrasound Skin Lifting
Ultherapy PRIME
Why we chose it
We selected Ultherapy PRIME® for its established clinical history and unique ability to deliver microfocused ultrasound with real-time imaging. This allows treatment to be precisely targeted to the appropriate tissue depth, supporting a natural-looking lift and progressive collagen remodelling.
Clinical evidence
Ultherapy has an extensive clinical history, with published research supporting its use for non-invasive lifting and improvement of skin laxity. Its effects are achieved by stimulating the skin’s natural collagen-remodelling response, with results developing progressively over time.
Regulatory status & provenance
Ultherapy PRIME is an FDA 510(k)-cleared Class II medical device. The original Ulthera System received FDA clearance in 2009, establishing the technology as a non-invasive focused ultrasound treatment for aesthetic skin lifting. The current PRIME platform received subsequent FDA clearances, including in 2024 and 2025.
Technology differentiation
Ultherapy PRIME combines microfocused ultrasound energy with real-time ultrasound visualisation. This allows the practitioner to see the tissue layers beneath the skin and precisely position treatment energy at the intended depth, including the deeper structural layer involved in skin lifting.
Safety
Ultherapy is a non-invasive treatment with an established safety profile. Temporary redness, swelling, tenderness or sensitivity may occur following treatment. Some patients may experience temporary discomfort or transient nerve-related effects. Treatment is carefully individualised according to anatomy and clinical indication.
Results
Ultherapy is designed to improve skin laxity, definition and firmness, particularly around the brow, jawline, chin and neck. Results develop gradually as collagen is remodelled, with improvement becoming more apparent over the following 2–3 months and potentially lasting a year or longer, depending on the individual.
Sessions & Recovery
Treatment assessed according to individual ageing and skin laxity.
Downtime: There is generally no planned downtime. Mild redness, swelling or tenderness may occur temporarily, and most patients can return to normal activities immediately. Ultherapy is typically performed as a single treatment, with the need for further treatment assessed individually.
Foundational to Zarya Lift and used within Zarya Transformation.
Structural Skin Tightening
XERF
Why we chose it
We selected XERF for its innovative approach to non-invasive skin tightening. Unlike conventional monopolar RF systems using a single frequency, XERF combines 6.78 MHz and 2 MHz to deliver controlled energy at different tissue depths, supporting both immediate contraction and longer-term collagen remodelling.
Clinical evidence
Emerging clinical evidence supports XERF for improving skin laxity, firmness and overall skin quality. Clinical studies have demonstrated visible improvements following treatment, with results continuing to develop as new collagen is formed and remodelled.
Regulatory status & provenance
XERF is an FDA 510(k)-cleared medical device, with clearance granted in August 2025. The device is manufactured by Lutronic Corporation, South Korea.
Technology differentiation
XERF is a multifrequency monopolar radiofrequency system combining 6.78 MHz and 2 MHz energy to target different tissue depths. Intelligent energy delivery and integrated cooling allow treatment to be precisely controlled while maintaining patient comfort and protecting the skin surface.
Safety
XERF is a non-invasive treatment requiring no needles or surgical intervention. Temporary warmth, redness or mild sensitivity may occur following treatment. There is generally no planned downtime, allowing patients to return to their normal activities immediately.
Results
XERF is designed to improve the appearance of skin laxity, facial firmness, jawline definition, fine lines and overall skin quality. Some tightening may be visible shortly after treatment, with further improvement developing progressively over the following weeks and months as collagen remodelling occurs.
Sessions & Recovery
We typically recommend 2 sessions approximately 4 weeks apart, with the treatment plan individualised according to the degree of laxity and the patient’s response.
Downtime: There is generally no planned downtime. Mild redness, warmth or tenderness may occur temporarily and usually settles quickly.
Core to Zarya Tighten.
Advanced Fractional Skin Resurfacing
UltraClear
Why we chose it
We selected UltraClear® for its advanced approach to skin resurfacing, combining the precision of a 2910 nm fibre laser with controlled fractional ablation. It allows treatment to be tailored from a subtle skin refresh to more intensive resurfacing, depending on the patient’s concerns and desired recovery.
Clinical evidence
Clinical studies have demonstrated improvements in photoageing, fine lines, skin texture and acne scarring following treatment with the 2910 nm fibre laser. Published studies report visible improvement with generally mild-to-moderate post-treatment skin responses and favourable patient satisfaction.
Regulatory status & provenance
UltraClear is an FDA 510(k)-cleared Class II medical laser system. The original platform received FDA clearance in December 2021, with expanded indications receiving further clearance in May 2024. The device is manufactured by Acclaro Corporation, USA.
Technology differentiation
UltraClear uses a 2910 nm erbium-doped fluoride fibre laser, a wavelength highly absorbed by water in the skin. Its proprietary 3DIntelliPulse® technology precisely controls ablation and coagulation, allowing resurfacing with reduced residual heat compared with conventional ablative laser approaches. Multiple treatment depths and modes allow the treatment to be customised to the patient’s skin and clinical objectives.
Safety
UltraClear is an ablative laser treatment and therefore produces a controlled skin-healing response. Depending on treatment intensity, temporary redness, swelling, warmth, pinpoint bleeding, sensitivity and superficial crusting or peeling may occur. Treatment parameters are carefully individualised according to skin type, indication and desired downtime.
Results
UltraClear is designed to improve skin texture, tone, pigmentation, fine lines, wrinkles, acne scars and signs of photodamage, while stimulating longer-term collagen remodelling. Results develop progressively as the skin heals and remodels.
Sessions & Recovery
The number of treatments depends on the indication and treatment intensity. Some patients achieve meaningful improvement after a single treatment, while a course may be recommended for more advanced concerns such as scarring or significant photodamage.
Downtime: Recovery is treatment-dependent. Superficial treatments may involve 1–2 days of minimal downtime, moderate resurfacing approximately 3–5 days, while deeper treatments may require 5–10 days. Redness, peeling and temporary sensitivity are expected during the healing period.
Used within Zarya Renew, Zarya Glow and the Zarya Pigmentation Pathway.
Precision Pigment & Skin Rejuvenation
CUTERA Pico Enlighten
Why we chose it
We selected CUTERA Pico enlighten for its advanced picosecond technology and exceptional precision in treating unwanted pigmentation while supporting a more even, refined complexion. Its versatility allows treatment to be carefully tailored to the individual skin and concern.
Clinical evidence
Picosecond laser technology has an established and growing body of clinical evidence supporting its use for benign pigmentation and skin rejuvenation. Clinical studies demonstrate improvements in pigmentation, skin tone and texture with generally favourable tolerability.
Regulatory status & provenance
CUTERA Enlighten is an FDA 510(k)-cleared Class II medical laser platform, developed and manufactured by CUTERA, Inc., USA. The original enlighten platform received FDA clearance in 2014, with subsequent generations receiving additional clearances. The manufacturing date of an individual device is identified by its device serial-number documentation.
Technology differentiation
Enlighten combines picosecond and nanosecond pulse technology with multiple wavelengths, allowing precise targeting of pigment at different depths. Its Micro Lens Array (MLA) technology can additionally create a controlled fractional effect, supporting improvements in skin texture and overall skin quality.
Safety
The ultra-short picosecond pulses deliver energy in extremely brief bursts, allowing pigment to be targeted with limited thermal impact on surrounding tissue. Temporary redness, mild swelling and darkening or flaking of treated pigment can occur. Treatment settings are carefully individualised according to skin type and clinical indication.
Results
Treatment can visibly improve sun damage, age spots, freckles and uneven pigmentation, while supporting a clearer, more luminous and uniform complexion. Results develop progressively as fragmented pigment is naturally cleared by the body.
Sessions & Recovery
A course of 2–4 sessions, generally spaced 2–4 weeks apart, may be recommended depending on the indication and individual response.
Expected downtime: Mild redness and swelling may occur temporarily. Pigmented areas may darken before gradually fading or lightly flaking over the following days. Most patients experience minimal downtime.
Central to Zarya Pigmentation Reset and the Zarya Pigmentation Pathway.
Advanced Vascular, Acne & Pigment Laser Technology
Excel V+
Why we chose it
Clinical evidence
Excel V+ utilises the well-established 532 nm KTP and 1064 nm Nd:YAG wavelengths, which have extensive clinical application in vascular and pigmentary conditions. Published clinical studies demonstrate significant improvements in facial erythema and vascular lesions, with a favourable tolerability profile when appropriately selected and performed.
Regulatory status
Excel V+ is an FDA-cleared, CE-marked Class II medical laser, developed and manufactured by Cutera, Inc., USA, and in clinical use since 2011.
What differentiates the technology
The combination of 532 nm and 1064 nm wavelengths allows treatment of both superficial and deeper vascular structures, while adjustable parameters enable treatment to be precisely matched to the individual patient and indication.
Safety
excel V+ is designed for controlled, precise delivery of laser energy, with integrated contact cooling to help protect the skin’s surface during treatment. Settings are tailored to each patient’s skin type, concern and treatment area.
Temporary redness and swelling are common after treatment and usually settle within hours to a few days. Some treatments may cause short-lived bruising. Less commonly, blistering or changes in pigmentation can occur. A thorough consultation and skin assessment before treatment, combined with experienced clinical care, help minimise these risks
Results
Treatment can produce clinically meaningful improvement in facial redness, rosacea, telangiectasia, vascular lesions, acne and selected pigmentation, with results dependent on the condition, skin characteristics and treatment protocol. A course of treatments may be recommended where clinically appropriate.
Sessions & Recovery
A course of 3–6 sessions, typically spaced approximately 4 weeks apart, is recommended depending on the indication and individual response.
Expected downtime: Mild redness and swelling may occur for 24–48 hours. Treated lesions may temporarily darken, crust or form small scabs as they respond to the laser. These effects generally settle over several days as the skin heals.
Underpins Zarya Calm and the Zarya Redness Pathway.
Advanced Non-Ablative Skin Revitalisation
Laser Genesis
Why we chose it
We selected Laser Genesis for its gentle, non-ablative approach to skin rejuvenation. Combining 532 nm and 1064 nm wavelengths allows us to tailor treatment to individual concerns, from superficial redness and vascular imperfections to deeper dermal rejuvenation and collagen stimulation.
Clinical evidence
Both the 532 nm and 1064 nm wavelengths have established clinical applications in vascular treatment and non-ablative skin rejuvenation. Treatment can improve redness, uneven tone, fine lines, skin texture and overall skin quality, with minimal disruption to the skin surface.
Technology differentiation
The 532 nm wavelength is particularly suited to superficial vascular concerns and redness, while the 1064 nm Nd:YAG wavelength penetrates deeper into the dermis, creating controlled thermal stimulation that supports collagen remodelling. This combination allows treatment to be precisely adapted to the indication and individual skin characteristics.
Safety
Laser Genesis is non-invasive and non-ablative, with no removal of the skin surface. Treatment is generally well tolerated. Temporary warmth and mild redness may occur and usually settle shortly after treatment.
Results
Laser Genesis can improve the appearance of facial redness, superficial vessels, uneven pigmentation, fine lines, enlarged pores and skin texture. With a course of treatments, the skin can appear smoother, clearer, more even and more luminous.
Sessions & Recovery
A course of 3–6 sessions, typically spaced 2–4 weeks apart, may be recommended depending on the indication and individual response.
Downtime: There is generally no planned downtime. Mild redness or warmth may occur immediately following treatment, and most patients can return to normal activities straight away.
Regulatory Status
Laser Genesis is a treatment protocol developed by Cutera, Inc., USA, and performed at Zarya on the excel V+ laser platform. excel V+ is an FDA 510(k)-cleared Class II medical laser, developed and manufactured by Cutera, Inc., and launched in 2019 as the latest generation of the excel V platform.
Advanced Cellulite & Skin Firming
EMTONE
Why we chose it
We selected EMTONE for its unique combination of monopolar radiofrequency and Targeted Pressure Energy (TPE). By addressing both the thermal and mechanical components associated with cellulite, the treatment is designed to improve skin firmness, texture and the visible appearance of cellulite.
Clinical evidence
Clinical studies have demonstrated improvements in cellulite appearance, skin elasticity and tissue quality following a course of treatment. Results develop progressively as the treated tissue responds to the combined thermal and mechanical stimulation.
Regulatory status & provenance
EMTONE is a Class II medical device with FDA clearance for specified indications, including temporary reduction in the appearance of cellulite. The technology is developed and manufactured by BTL Industries, with European manufacturing.
Technology differentiation
EMTONE uniquely combines radiofrequency energy with Targeted Pressure Energy simultaneously. Radiofrequency delivers controlled thermal energy to the tissue, while mechanical pressure stimulates the underlying connective tissue. This dual approach is designed to address multiple contributing factors of cellulite within a single treatment.
Safety
EMTONE is a non-invasive treatment with no needles or surgical intervention. Treatment may produce a sensation of warmth and rhythmic pressure or vibration. Temporary redness, mild sensitivity or tenderness may occur, but there is generally no planned downtime.
Results
EMTONE is designed to improve the appearance of cellulite, skin laxity and uneven skin texture, particularly on areas such as the thighs, buttocks and abdomen. Improvements develop progressively and can continue for several weeks following treatment.
Sessions & Recovery
A course of 4 treatments, typically performed approximately one week apart, is commonly recommended. The treatment plan is individualised according to the area treated and degree of cellulite or skin laxity.
Downtime: There is generally no downtime, and normal activities can be resumed immediately. Mild redness, warmth or tenderness may occur temporarily following treatment.
Used within body-focused plans and Zarya Transformation.
Advanced LED Phototherapy
Dermalux Tri-Wave MD
Why we chose it
Clinical evidence
LED phototherapy has an established body of clinical research supporting its use in skin rejuvenation, acne, inflammation and wound healing. Dermalux combines three specific wavelengths, each selected for a distinct biological response.
Regulatory status & provenance
Dermalux Tri-Wave MD is a Class IIa medical device and is FDA 510(k)-cleared. The device is developed and manufactured by Aesthetic Technology Ltd in the United Kingdom.
Technology differentiation
Tri-Wave MD combines three clinically established wavelengths:
415 nm Blue — targets acne-causing bacteria and supports clearer skin.
633 nm Red — supports collagen production, skin repair and visible rejuvenation.
830 nm Near-Infrared — penetrates more deeply to support cellular repair, circulation and tissue recovery.
The wavelengths can be used individually or in combination, allowing treatment to be tailored to the skin’s specific needs.
Safety
LED phototherapy is non-invasive, non-thermal and generally very well tolerated. There is no skin abrasion or controlled injury, making it suitable for regular treatments and for supporting the skin before or after more intensive procedures. Temporary warmth or mild redness may occur but usually settles quickly.
Results
Dermalux can improve the appearance of acne, redness, inflammation, uneven skin tone, fine lines and overall skin quality. With repeated treatments, the skin can appear calmer, clearer, more hydrated and more luminous.
Sessions & Recovery
A course of 4–6 sessions, typically performed 1–2 times per week, may be recommended depending on the indication and individual skin response.
Downtime: None. Treatment is painless, non-invasive and patients can return to normal activities immediately.
Built into recovery across Zarya Glow, Zarya Calm and post-procedure aftercare.
Cleansing & Hydration
Hydrafacial
What it is
Hydrafacial is an advanced skin health treatment that cleanses, exfoliates, extracts and infuses the skin in a single session.
How it works
A vortex handpiece uses fluid technology to loosen and lift debris from the pores while simultaneously delivering serums into the skin. Because extraction is achieved through gentle suction rather than manual pressure, the skin is left calm rather than traumatised. Serums are selected according to your skin’s needs — hydrating, brightening or clarifying.
What we use it for
- Congestion, blackheads and enlarged pores
- Dehydration and dullness
- Skin preparation before an event
- Ongoing maintenance between clinical treatments
What to expect
- Comfortable and often described as relaxing
- Zero downtime — skin looks brighter immediately
- Ideal monthly or six-weekly as part of a longer-term plan
A maintenance layer within Zarya Glow and most ongoing skin strategies.
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