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PZLASER RevitaELF

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PZLASER RevitaELF

✓ Certified Professional Seller

PZLASER Dermatology & Aesthetics

PZLASER RevitaELF

Built for hair regrowth and aesthetic skin treatment, with interchangeable non-invasive and fractional mode tips.

The RevitaELF ships in a single wooden case containing the laser cabinet, touchscreen console, two treatment handpieces, and the standard tip set (hair-loss non-invasive and fractional tips, skin-rejuvenation non-invasive and fractional tips). Assembled, the cabinet occupies a clinic footprint of approximately 600 × 600 mm with the four mobile castors and requires standing clearance for the articulated arm. Confirm room dimensions and electrical position at site survey before delivery.

Sections

Fractional Lasers

Categories

Dermatology & Aesthetics

Condition

Perfect

Origin

China

Seller Type

Certified Professional Seller

Size:

920 × 720 × 1320 mm

CE & ISO Certified

Global Shipping

Supplier: Medigear

The RevitaELF is built around an erbium-glass fiber laser at 1565nm wavelength — the same wavelength class established by the Lumenis ResurFX and FoLix platforms for non-ablative fractional applications. At 1565nm, the laser is absorbed primarily by tissue water, creating controlled micro-thermal damage in the dermis without ablating the epidermis. This drives collagen regeneration to repair acne scars and fine lines, supports rapid recovery because the stratum corneum stays intact, and — when used for hair regrowth — creates deep micro-channels that improve scalp circulation, stimulate collagen production in hair follicles, and assist topical drug penetration.

The treatment platform supplies four interchangeable tips across two clinical pathways. The hair-loss pathway offers a non-invasive mode tip for general scalp stimulation and a fractional mode tip for deeper micro-channel creation. The skin-rejuvenation pathway offers the same non-invasive and fractional mode tips, sized and configured for facial and body aesthetic indications. Tips are quick-change at the handpiece, supporting back-to-back hair and skin protocols in a single session if the clinic operates blended aesthetic packages.

Treatment is operated from the touchscreen control console mounted at the top of the cabinet. The interface includes preset protocols for typical hair-loss and skin-rejuvenation indications, manual energy adjustment for clinician control, treatment-area tracking, and patient-record fields. PZLASER positions the RevitaELF as the first fractional laser in China cleared for hair-loss treatment by the Chinese regulator, with published clinical outcomes showing a 20% increase in hair count per cm², 17% additional follicular units per cm², and 90% patient satisfaction scores. The standard treatment course is 3–6 thirty-minute sessions to achieve results, with each session typically scheduled 2 weeks apart per the published 1565nm NAFL clinical protocols. CE marking documentation, customs paperwork, and UK distribution support are confirmed at quotation.

The PZLASER RevitaELF serves UK aesthetic clinics, dermatology practices, hair-restoration centres, and cosmetic surgery clinics offering 1565nm non-ablative fractional laser treatment. The dual-pathway tip set covers both hair-regrowth and skin-rejuvenation protocols on a single platform, supporting practices that run blended aesthetic packages and want to consolidate equipment spend across multiple indications.

In hair-loss treatment, the RevitaELF addresses androgenetic alopecia (male and female pattern hair loss), traction alopecia in early stages, and certain non-scarring alopecia areata cases following clinician assessment. The fractional mode tip creates the micro-channels through which scalp circulation improves and topical drug penetration is enhanced — supporting combination protocols with minoxidil, finasteride, or platelet-rich plasma where the clinician considers these appropriate. Published research suggests the wavelength produces hair-count outcomes comparable to or better than topical minoxidil in selected patient populations.

In skin rejuvenation, the device addresses fine lines and wrinkles, photoaging, acne scarring (rolling, boxcar, and ice-pick subtypes following clinician triage), surgical and traumatic scar revision, post-inflammatory hyperpigmentation, stretch marks across the abdomen and thighs, and enlarged facial pores. The fractional mode tip targets deeper dermal remodelling; the non-invasive mode tip suits milder rejuvenation indications and patients who prefer minimal downtime.

For combination aesthetic-and-hair clinics, the platform supports sequential treatment of patients across both indication groups, simplifying capacity planning and capital equipment justification. Practices integrating the RevitaELF into broader treatment menus typically pair it with topical therapy protocols, microneedling alternatives for milder cases, and consultation pathways that include realistic expectation-setting on the typical 3–6 session response curve.

1565nm Erbium-Glass Fiber Wavelength

The 1565nm wavelength sits at the established sweet-spot for non-ablative fractional treatment — absorbed by water in the dermis to create controlled micro-coagulation while leaving the epidermis intact. This is the same wavelength class as the Lumenis ResurFX and FoLix platforms.

Dual Treatment Pathway on One Platform

Hair-regrowth and skin-rejuvenation pathways share the same laser source and console, with interchangeable tips selecting the clinical mode. This reduces capital equipment cost compared with separate hair-loss and skin lasers and consolidates training and maintenance.

Non-Invasive and Fractional Tips Per Pathway

Each clinical pathway carries both a non-invasive mode tip and a fractional mode tip — four tips in total — supporting clinician-selected treatment depth based on patient tolerance, indication severity, and downtime expectations.

Minimal Recovery Downtime

Because the epidermis stays intact during non-ablative treatment, patients typically return to normal activity the same day with only mild erythema lasting hours. This makes the platform suitable for treatment scheduling around patients' working and social commitments.

Established Clinical Evidence Base

1565nm non-ablative fractional laser is supported by independent peer-reviewed research in journals including the Journal of Cosmetic Dermatology and Lasers in Medical Science, covering androgenetic alopecia, acne scarring, enlarged facial pores, and aged-skin remodelling.

Touchscreen Console with Preset Protocols

The mounted touchscreen console carries preset protocols for typical hair-loss and skin-rejuvenation indications, manual energy adjustment for clinician override, treatment-area tracking, and patient-record fields.

Four-Castor Mobile Cabinet

The cabinet rolls between treatment rooms on four castors, supporting practices with multiple operatories sharing the platform. Castors lock in position for treatment delivery.

CE Marking and UK Distribution Support

Medigear.uk supplies the device with CE marking documentation and UK distribution support. UKCA status and the buyer's clinic regulatory position are confirmed at quotation.

Published Manufacturer Outcomes

PZLASER cites manufacturer outcomes of 20% increase in hair count per cm², 17% additional follicular units per cm², and 90% reported patient satisfaction. Independent clinical outcomes vary by patient and baseline severity.

Erbium-Glass Fiber Laser Source at 1565nm

The laser source is an erbium-glass fiber laser operating at 1565nm wavelength — the established non-ablative fractional wavelength absorbed by tissue water.

Non-Invasive Mode Hair-Loss Tip

A handpiece-mounted tip for general scalp stimulation in hair-regrowth treatment, suited to patient-tolerance-sensitive cases and earlier-stage hair loss.

Fractional Mode Hair-Loss Tip

A handpiece-mounted tip that creates deeper micro-channels through the scalp dermis to support topical drug penetration and follicular stimulation.

Non-Invasive Mode Skin Tip

A handpiece-mounted tip for milder skin rejuvenation indications including fine-line softening and post-treatment maintenance.

Fractional Mode Skin Tip

A handpiece-mounted tip for deeper dermal remodelling indications including acne scarring, stretch marks, and aged-skin remodelling.

Touchscreen Control Console

The console sits at the top of the cabinet on an adjustable mount, with a touchscreen interface for protocol selection, energy adjustment, treatment-area tracking, and patient records.

Preset Treatment Protocols

The console carries preset protocols for typical hair-loss and skin-rejuvenation indications. Clinicians can use the preset or adjust energy manually.

Manual Energy Adjustment

Energy delivery is adjustable across the published 1565nm therapeutic range, supporting clinician-selected dosing per patient and indication.

Treatment-Area Tracking

The console logs the treated area through the session for clinical record-keeping and follow-up reference.

Patient-Record Fields

Patient identification, treatment history, and session notes are stored on the console for review at subsequent sessions.

Four Mobile Castors with Locks

The cabinet rolls between treatment rooms on four castors and locks in position for treatment delivery. The cabinet is designed for clinic-floor mobility rather than fixed installation.

Quick-Change Handpiece Tips

The tips snap on and off the handpiece for rapid pathway changes between hair-loss and skin-rejuvenation protocols within a single session.

Hospital-Grade Mains Supply

The cabinet requires a hospital-grade single-phase mains supply at 220–240 V, 50 Hz for UK installation. Specific amperage is on the technical data sheet.

Laser Safety Compliance Requirements

Use of the device requires laser-safety signage, door interlock, wavelength-matched eyewear for operator and patient, and consultation with the clinic's MHRA-compliant Laser Protection Adviser.

Standard Session Duration

Each treatment session is approximately 30 minutes from setup to recovery counselling. Course recommendation is 3–6 sessions at 2-week intervals.

Standard Configuration

The standard package includes the cabinet, console, two handpieces, the four-tip set (hair-loss non-invasive and fractional, skin-rejuvenation non-invasive and fractional), foot switch, operating manual, and CE marking documentation.

The PZLASER RevitaELF is a strong fit for UK aesthetic clinics, dermatology practices, and hair-restoration centres looking to consolidate hair-regrowth and skin-rejuvenation treatment on a single 1565nm non-ablative fractional laser platform. Its erbium-glass fiber laser source, dual-pathway interchangeable tip set, touchscreen console with preset protocols, and mobile four-castor cabinet cover the daily clinical demands of androgenetic alopecia treatment, acne scar revision, stretch-mark management, fine-line softening, and aged-skin remodelling. The established 1565nm clinical evidence base supports the wavelength's efficacy across both hair and skin indications. Medigear.uk distributes the RevitaELF across the United Kingdom with CE marking documentation, customs and installation support, and warranty cover through PZLASER's UK partner network. Contact Medigear.uk for quotations, clinic-environment survey support, training referral to PZLASER's UK training partners, and configuration options.

FAQ

Frequently Asked Questions

Everything buyers need to know about sourcing medical equipment through MediGear.

At 1565nm the laser is absorbed primarily by tissue water rather than haemoglobin or melanin, so it deposits controlled thermal energy in the mid-to-deep dermis without ablating the epidermis. This creates micro-coagulation zones surrounded by intact tissue, which triggers a wound-healing response that drives collagen regeneration, neocollagenesis, and follicular stimulation. Because the epidermis stays intact, downtime is minimal compared with ablative fractional lasers operating at 2940nm or CO2 wavelengths.

The Lumenis ResurFX and FoLix platforms use the same 1565nm erbium-glass fiber laser class and are the FDA-cleared comparable devices for skin resurfacing (ResurFX) and hair-loss treatment (FoLix). The PZLASER RevitaELF is a separate Chinese-manufactured platform at the same wavelength with its own treatment tip set, control console, and clinical protocols. The RevitaELF is not a Lumenis product and is not manufactured under licence; it is positioned as an independent 1565nm fractional laser supplied through PZLASER's UK distribution partners including Medigear.uk.

Medigear.uk confirms CE marking documentation, declaration of conformity, and UKCA status at quotation. UK distribution of medical and aesthetic lasers requires Medical Devices Regulations 2002 (as amended) compliance and, for clinics performing the treatments, registration with the Care Quality Commission for treatments designated as regulated activities. Buyers should confirm both the device's marking status and their clinic's regulatory position before committing to the purchase.

PZLASER cites manufacturer outcomes of approximately 20% increase in hair count per cm², 17% additional follicular units per cm², and 90% reported patient satisfaction. Independent published research on 1565nm non-ablative fractional laser treatment of androgenetic alopecia — including a 2024 randomised study against 5% minoxidil — supports the wavelength's efficacy for hair regrowth at typical settings of 10 mJ and 250 spots/cm² across 4 sessions at 2-week intervals. Clinical outcomes vary by patient, baseline hair-loss stage, and treatment compliance.

The skin-rejuvenation pathway is indicated for fine lines and wrinkles, post-inflammatory and sun-induced pigmentation, stretch marks, acne scarring, surgical and traumatic scar revision, and general skin texture improvement. Published evidence supports 1565nm non-ablative fractional treatment for enlarged facial pores, acne scarring, and aged skin remodelling. The fractional mode tip targets deeper dermal remodelling; the non-invasive mode tip is suited to milder rejuvenation indications and patient-tolerance-sensitive cases.

PZLASER's protocol recommends 3–6 sessions of approximately 30 minutes each to achieve results, with sessions typically scheduled 2 weeks apart in line with published 1565nm NAFL clinical research. Hair-regrowth response is usually observed from session 3 onwards with continued improvement over the following 3–6 months. Maintenance sessions are recommended every 3–6 months thereafter depending on the underlying hair-loss aetiology and the patient's clinical response.

1565nm non-ablative fractional treatment is generally well tolerated. The handpiece may include a contact-cooling tip or topical anaesthetic cream may be applied 30 minutes before higher-energy passes. Patients typically describe a warm prickly sensation rather than sharp pain. The non-invasive mode tip is considerably more comfortable than the fractional mode tip. Recovery downtime is minimal — most patients return to normal activity the same day with mild erythema lasting hours rather than days.

Standard fractional laser contraindications apply: active infection or inflammation in the treatment area, recent isotretinoin use (consult prescribing literature for current guidance), pregnancy, photosensitising medication, active herpes simplex outbreaks in the treatment field, history of keloid scarring, recent sun exposure or use of self-tan, and Fitzpatrick skin type concerns for higher-energy parameters. A thorough consultation and consent process is essential. Medigear.uk does not provide clinical training but can refer practices to PZLASER's training partners in the UK.

The RevitaELF ships with the standard PZLASER manufacturer warranty against quality defects, with terms and length confirmed at quotation. The erbium-glass fiber laser source carries its own service rating and replacement schedule. Medigear.uk supports UK warranty fulfilment through PZLASER's authorised UK service partner network. Extended warranty and biomedical service contracts can be added at order; specific terms are confirmed in the purchase agreement.

The RevitaELF requires a hospital-grade single-phase mains supply (220–240 V, 50 Hz for UK installation) with sufficient amperage for medical laser equipment — the exact rating is confirmed on the technical data sheet. The treatment room requires laser safety signage at the entrance, an interlock switch on the door, wavelength-matched laser safety eyewear for the operator and patient, and a non-reflective treatment-area environment. UK clinics should consult their MHRA-compliant Laser Protection Adviser before commissioning the device.