SkinPen incorporates sterile, single‑use needle cartridges and a protective BioSheath to prevent cross‑contamination. It is the first microneedling device to receive FDA clearance, confirming adherence to strict safety and performance criteria.

How many treatments are required?

Treatment frequency varies by indication. Most protocols involve multiple sessions spaced several weeks apart, determined by practitioner assessment.

Downtime is generally minimal. Temporary erythema or sensitivity may occur and typically resolves within a short period.

Is SkinPen suitable for all skin types?

Yes. The device is appropriate for all Fitzpatrick skin types and can be used year‑round under professional supervision.

How does SkinPen works?

SkinPen creates controlled microchannels that activate the body’s wound‑healing response. This process supports collagen and elastin production, improving texture and reducing the appearance of wrinkles and scars.

SkinPen^®

Name: SkinPen®
Brand: DUBIMED
Availability: InStock

FDA‑cleared microneedling device

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ABOUT SKINPEN®

SkinPen is a precision microneedling device developed by Crown Aesthetics and recognised as the first pen‑type system to receive FDA clearance. It is engineered to deliver uniform microchannel formation while maintaining epidermal integrity. The...

device is suitable for clinical environments requiring controlled, minimally invasive skin remodelling. SkinPen uses sterile, single‑use needle cartridges to create microchannels that initiate the body’s wound‑healing cascade. This process supports collagen and elastin production without thermal or chemical injury. The device is FDA‑cleared for the treatment of neck wrinkles (Fitzpatrick skin types II–IV) and facial acne scars in adults aged 22 and older. Its adjustable needle depth, cordless operation, and validated safety mechanisms support consistent performance across different anatomical regions. SkinPen is compatible with all skin types and can be used throughout the year under professional supervision.