All Dermabrasion devices must pass a series of requirements and guidelines in order to become approved by the FDA. Different types of these products and devices exist, therefore it is required of patients and medical professionals to check in with these guidelines in order to receive or provide safe skin rejuvenation.
Safety Guidelines
In the beginning of 1999, the US Food and Drug Administration, along with the US Department of Health and Human Services, plus other large regulatory groups, determined a set of requirements for Dermabrasion devices.
This rule set includes topics such as labeling and sterilization information. The guideline also mentions that in order for such device to serve as a safe and efficient tool, groups must specify their products purpose or intended use, along with an accurate and truthful statement about its capabilities.
Other Information
Before any type of Dermabrasion device becomes approved by the FDA, it must file for a request that contains the previously mentioned items along with even more information. Dermabrasion devices get used in multiple industries, making the information provided in these guidelines pivotal for patient safety.
Patients who undergo skin rejuvenation treatments that directly involve the use of Dermabrasion devices will better understand their level of safety or risk after asking their administering doctor or professional if the intended device has passed the FDA guidelines.
