Choosing FDA & CE Mark microneedling devices for your clinic
When it comes to choosing equipment for your clinic or private practice, choosing a CE Mark and FDA cleared microneedling devices is a good place to start.
Whether you’re looking to upgrade your current devices, or you’re new to microneedling, SkinPen is proven to be safe and effective in treatments.
In today’s blog, we’ll talk you through the benefits of choosing medical microneedling devices, and why SkinPen is the top choice for skin rejuvenation treatments.
Why add microneedling to your treatment portfolio?
It’s widely considered good practice to offer a wide variety of cosmetic treatments, especially when it comes to skin rejuvenation.
The beauty of microneedling as a medical treatment for skin improvement is that it offers a host of different treatments all using just one handheld device.
Medical microneedling treatments can help to improve a variety of skin related issues and concerns by encouraging new collagen to be produced. This in turn helps to create smoother, healthier looking skin.
Microneedling can help improve concerns ranging from acne scarring to fine lines, as well as minimising large pores. Being able to offer patients so many different aesthetic improvements from just one device means it’s a profitable addition to a clinic.
Treatments are quick to perform and with FDA cleared microneedling devices you can be confident your patients will be both safe and impressed with their skin rejuvenation results. SkinPen is also a CE Mark, Class 1 Medical Grade device, and not a cosmetic pen.
Why are these accreditations important?
FDA cleared is recognised across the world as a sign of quality and safety. CE Mark, Class 1 Medical Grade recognises the device as medical and not cosmetic.
It’s widely agreed that an FDA cleared device has been rigorously tested to ensure it’s a quality product. A quality product means reliability – and we think that’s worth shouting about at BioActiveAesthetics. The SkinPen went through over 90 FDA validations to achieve its clearance.
Having a CE Mark, Class 1 Medical Grade or FDA clearance means the device you choose, in this case SkinPen, is tried and tested to the highest standards. Experts ensure both the safety and efficacy of a device before approving it – this should give the user peace of mind when choosing medical and/or cosmetic devices.
Why choose SkinPen?
In 2018 SkinPen received full FDA clearance for use as a medical device. At the time, this was the first device of its kind to get this safety award alongside being awarded a CE Mark, Class 1 Medical Grade – we think this sets it as the gold standard in microneedling.
Today, in the UK market, SkinPen is the only mechanical microneedling device that holds FDA Clearance, CE Mark Class 1, ISO certified for quality and assurance and holds a BSI (British Standards Institute) Kitemark accreditation.
It’s effective on all skin types and allows for short treatment times, making it a cost-effective solution to add to your portfolio. On top of this, the recovery is swift as it’s only minimally invasive, making patient satisfaction high.
You can read other more in-depth posts about SkinPen on our website. Check out the blog section to see the latest articles we have available.
Getting more information
The BioActiveAesthetics team would be delighted to help you if you’re considering investing in microneedling technology. If you would like to learn more about choosing SkinPen, or you’d like to see a demonstration of the device in action, please contact us.
We are happy to discuss your needs and help you learn more about this exciting type of treatment. Don’t forget to read more about the device on the product pages.