IDROGENET SRL

IDrogenet Srl specializes in virtual-display rehabilitation systems focused on upper-limb therapy. Their devices include models with both powered and passive support, designed to assist in physical rehabilitation exercises through digital interfaces. These systems are intended for controlled movement and engagement, suitable for clinical or home-based use to support recovery and motor skill improvement.

IDrogenet Srl is based in the United States. Their devices are specifically designed and intended for use within the U.S., adhering to regulatory requirements applicable to their category of medical devices.

IDrogenet Srl’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of their Class I medical devices, which are intended for upper-limb rehabilitation.

IDrogenet Srl’s devices are classified as Class I medical devices. This classification is determined based on their intended use and risk profile, as defined by regulatory authorities. Class I devices generally pose minimal risk and often require less stringent regulatory oversight compared to higher-risk categories.