M & T SRL

M & T SRL specializes in dermatological laser systems, including diode laser systems and solid-state laser systems designed for professional use. They also produce cosmetic red-light phototherapy systems intended for skin treatments, hair removal, and related dermatological applications. These devices are tailored for clinical or professional settings rather than consumer use.

M & T SRL is based in the US, which means their devices are subject to US medical device regulations. Since their products fall under Class II classification, they must comply with FDA requirements for safety, performance, and labeling. The company’s devices are also listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and regulatory transparency.

M & T SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices under US regulatory oversight, ensuring compliance with mandatory identification standards for Class II devices like those produced by the company.

M & T SRL’s devices are classified as Class II under US medical device regulations. This classification applies to devices that generally pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. The company’s dermatological laser systems and phototherapy devices fall into this category due to their professional use and potential clinical impact.