RF microneedling and HIFU skin tightening platform
Certifications
Medical CE Certified professional RF microneedling and HIFU device (Europe/UK).
TGA registered in Australia (ARTG No. 371470) via CliniMed Aesthetics for FocusDual Branded systems.
Designed and manufactured in accordance with relevant medical electrical equipment safety and EMC standards as specified by Lynton Lasers.
Medical CE Certified professional RF microneedling and HIFU device (Europe/UK).
TGA registered in Australia (ARTG No. 371470) via CliniMed Aesthetics for FocusDual Branded systems.
Designed and manufactured in accordance with relevant medical electrical equipment safety and EMC standards as specified by Lynton Lasers.
RF microneedling and HIFU skin tightening platform
Description
The Lynton Focus Dual is a professional, medical CE-certified aesthetic device that combines fractional radiofrequency (RF) microneedling with High Intensity Focused Ultrasound (HIFU) to deliver non-surgical skin tightening, lifting, firming and resurfacing of the face and body. The system treats the skin at multiple levels (SMAS, reticular dermis, papillary dermis and epidermis) using ultra-fine insulated and non-insulated microneedles, vacuum-assisted delivery and Safety Assist Transducers (SAT) for HIFU, providing powerful yet controlled collagen stimulation with minimal discomfort and downtime. This listing refers to a pre-owned (used) Focus Dual unit offering RF microneedling and HIFU skin tightening treatments.
Bnefits
Combines RF microneedling and HIFU in one platform for comprehensive skin lifting, firming and resurfacing.
Non-surgical alternative to facelift with minimal downtime compared to invasive surgery.
Treats skin at every layer (SMAS, reticular dermis, papillary dermis and epidermis) for multi-level rejuvenation.
Ultra-fine microneedles (approx. 0.16 mm) with adjustable depths from 0.5–3.5 mm allow precise, customisable treatments for different skin concerns and areas.
Choice of insulated and non-insulated needle tips to optimise safety and efficacy across all Fitzpatrick skin types, including darker skin tones.
Vacuum suction technology stabilises the skin for safer, more accurate RF delivery and improved comfort, especially around delicate areas such as the eye region.
Safety Assist Transducers (SAT) for HIFU emit ultrasound in patterns designed to reduce surface tissue overlap, lowering the risk of post-inflammatory hyperpigmentation and discomfort.
Can target fine lines, wrinkles, skin laxity, acne and surgical scars, stretch marks, enlarged pores and localised fat deposits.
Results typically continue to improve for up to 12 weeks post-treatment as neocollagenesis progresses.
Clinical experience suggests results can last approximately 1–2 years, depending on patient lifestyle, age and maintenance top-up treatments.
Indications
Non-surgical skin tightening and lifting of the face and body
Localised body contouring and fat reduction in areas such as abdomen, flanks, thighs and upper arms
Composition
Fractional radiofrequency microneedling module with ultra-fine microneedles (approx. 0.16 mm diameter).
Insulated microneedle tips for targeted heating of deeper dermal layers while protecting the epidermis.
Non-insulated microneedle tips for volumetric heating along the full needle length to enhance collagen remodelling.
Adjustable microneedling depths typically ranging from 0.5 mm to 3.5 mm.
RF generator with multiple power levels (around 10 RF intensity settings) to tailor energy delivery.
HIFU module with multiple focal depths (face and body cartridges, including an optional 13 mm body cartridge for subcutaneous fat and deep tightening).
Safety Assist Transducers (SAT) for more uniform and safer HIFU energy distribution.
Vacuum suction technology for stabilising skin and needles during RF microneedling.
Integrated touchscreen user interface for parameter adjustment and treatment control.
Formulation
Energy-based device – no pharmacological or topical formulation.
Delivers thermal energy via RF microneedling in fractional patterns to induce controlled dermal injury and neocollagenesis.
Delivers focused ultrasound energy (HIFU) at controlled depths to contract the SMAS and deeper tissues, stimulating collagen and elastin production.
Configurable treatment parameters (needle depth, RF level, HIFU focal depth) allow protocol customisation for different anatomical areas and indications.
Packaging
Main Focus Dual console containing RF microneedling and HIFU control systems.
RF microneedling handpiece with interchangeable microneedle tip cartridges (e.g. 10-pin and 25-pin tips).
HIFU handpieces with a range of cartridges for different focal depths, including optional body contouring cartridge (e.g. 13 mm).
Power cables and footswitch (where applicable), plus manufacturer-supplied accessories as per original configuration.
Supplied new with user manual, training and support from Lynton or regional distributor; used units may include components and accessories as specified by the seller.
Usage
For professional use only by appropriately trained medical and aesthetic practitioners familiar with RF microneedling and HIFU technologies and local regulations.
Perform a full medical history, skin assessment and suitability check before treatment; obtain informed consent.
Select treatment mode (RF microneedling, HIFU or combination) according to indication, skin type and treatment area.
For RF microneedling: cleanse and prepare the treatment area; apply topical anaesthetic if required and remove thoroughly before treatment.
Set needle depth (approximately 0.5–3.5 mm) and RF intensity based on indication, anatomical location and skin thickness, following manufacturer training guidelines.
Use the vacuum-assisted RF microneedling handpiece to stamp the skin in overlapping passes, ensuring even coverage without excessive overlap of energy.
For HIFU: mark treatment zones if recommended; select appropriate cartridge and focal depth (e.g. SMAS-level, mid-dermis or subcutaneous for body contouring).
Apply ultrasound gel and deliver HIFU shots according to the treatment protocol, monitoring patient comfort and avoiding bony prominences where advised.
Post-treatment: apply soothing products and broad-spectrum SPF, and provide aftercare instructions (e.g. avoid heat exposure, strenuous exercise and active topicals immediately post-procedure).
Typical treatment plans involve 1–3 sessions spaced about 4–6 weeks apart, with optional maintenance sessions approximately once or twice per year, as guided by clinical response and manufacturer recommendations.
Contraindications
Not publicly listed
Adverse Effects
Not publicly listed
Storage Conditions
Refer to the official Lynton Focus Dual user manual for specific storage and handling conditions.
In general, store the device and its handpieces in a clean, dry clinical environment, protected from dust, moisture, extreme temperatures and mechanical shock.
Ensure the system is disconnected from mains power before cleaning, maintenance or relocation, following manufacturer instructions.
Duration
Results generally evolve over 4\u201312 weeks after the final session as new collagen forms, and may last approximately 1\u20132 years depending on individual factors and maintenance.
Onset
Some patients notice immediate tightening and improved skin feel, with progressive improvement over the subsequent 4\u201312 weeks as neocollagenesis and tissue remodelling occur.
