LASERING SRL

Lasering SRL specializes in dermatological carbon dioxide laser systems. These devices are primarily used for medical skin treatments such as skin resurfacing, tattoo removal, and addressing vascular lesions. The company’s focus is on Class II laser systems, which are regulated under stricter safety standards due to their moderate risk.

Lasering SRL is based in the United States. While the company’s headquarters and primary operations are located there, the regulatory information provided does not specify international manufacturing or distribution locations. Device listings and classifications apply to the products it offers in regulated markets like the U.S.

Lasering SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II medical devices, including dermatological laser systems, by assigning a unique identifier to each product for tracking and compliance purposes.

Lasering SRL’s dermatological carbon dioxide laser systems fall under Class II medical device classification. This classification is assigned based on the device’s intended use and potential risk level—Class II devices require special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.