Get Skinpen Consent Form

Avoid Shaving the treatment area. You may closely shave 1 day prior to your treatment. Come to your visit with freshly cleansed skin, meaning no lotion, oil makeup, powder, perfume or sunscreen. If needed you may cleanse your face at your appointment.

Skin Care Consent Form is used to acquire approval from the client who chooses to avail of the service of the dermatology clinic. In a dermatology clinic, there are invasive and non-invasive procedures which is why a signed consent form is needed from the client so that both parties will be protected legally.

At-home microneedling devices also only superficially affect the skin—they penetrate just its outer layer (the stratum corneum or epidermis), reaching 0.25 mm deep. Professional devices can go deeper (2 mm to 3 mm deep), reaching not only the epidermis but also the dermis, a deeper layer of skin.

Professional Microneedling pens typically have adjustable needles that range from 0.25mm to 2.5mm. For wrinkles and fine lines, you will need 1.0mm to 2.5mm needle depth. Acne scars will require at least 1.5mm.

SkinPen Microneedling is a more standard microneedling treatment. In fact, it is the only FDA-approved microneedling device available on the market. It has tiny needles at the end of the pen-like device that puncture the top layer of the skin.

While deeper procedures can help remodel scar tissue from stretch marks or acne, subcutaneous scarring can be caused if pushed too deep. This would be similar in nature to a third degree burn and not the level for estheticians to be entering unless working with a physician.

It uses adjustable length, disposable straight needles to penetrate at a 90-degree angle, at a customizable depth of 0.25 to 2 millimeters. This adjustability allows for differences in skin thickness and skin types, as well as enhanced safety. The FDA has also cleared SkinPen for the treatment of wrinkles on the neck.

In short, under FDA guidelines, estheticians can only use microneedling devices of less than 0.3 mm and only those that do not make medical claims. If a device is less than 0.3 mm but makes medical claims, it also cannot be approved for sale or use.