Frequently Asked Questions

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  Treatment outcomes vary depending on the injectable product used, the treatment protocol, and individual patient factors. Many practitioners use MicronJet™ as part of skin rejuvenation, hydration, and regenerative treatment plans where visible improvements may develop over the days and weeks following treatment. The device itself does not determine treatment results, but facilitates precise intradermal delivery.

  The longevity of results depends on the formulation administered, the treatment area, and individual patient characteristics. As MicronJet™ is a delivery device, treatment duration and maintenance schedules are determined by the injectable product and practitioner-led treatment plan.

  MicronJet™ is designed for use by qualified healthcare professionals and may be incorporated into a wide range of aesthetic and dermatological procedures. Patient suitability should always be assessed by the treating practitioner, taking into consideration medical history, treatment goals, and any contraindications associated with the injectable product being used.

  As with any injection-based procedure, temporary treatment-site reactions such as redness, swelling, tenderness, or minor bruising may occur. The type and severity of any side effects can vary depending on the treatment performed and the injectable formulation administered. Patients should always follow the aftercare advice provided by their practitioner.

  Yes. MicronJet™ is compatible with a variety of practitioner-selected injectable formulations used in aesthetic and regenerative medicine, including skin boosters, mesotherapy solutions, PRP, exosomes, and other intradermal treatment protocols. Product selection should always be based on clinical judgement and manufacturer guidance.

  Aftercare recommendations will vary depending on the treatment performed and the product administered. Patients are typically advised to follow practitioner instructions carefully, which may include avoiding excessive sun exposure, strenuous exercise, heat treatments, and potentially irritating skincare products for a short period after treatment.

Both devices utilise the same patented microneedle technology but are designed for different depths of intradermal delivery. The 0.6mm device is often selected for very superficial treatments and delicate areas, while the 0.8mm device may be preferred where slightly deeper dermal placement is required. The appropriate device should be chosen based on the treatment indication and practitioner preference.

 The choice between MicronJet™ 0.6mm and 0.8mm depends on the treatment objective, injection depth required, and the area being treated. Qualified practitioners should select the most appropriate device according to their clinical assessment and treatment protocol.