Recovery Force, LLC

Recovery Force, LLC specializes in intermittent venous compression devices. Their portfolio includes systems that combine movement and pneumatic compression, such as the Movement and Compressions System (MAC) and the RF1400 Active Compression Wrap. These devices are designed to enhance venous circulation and reduce swelling in patients, particularly those recovering from surgery or dealing with chronic venous insufficiency.

Recovery Force, LLC is based in the United States. Since the company operates within the US regulatory framework, its devices are authorised through the FDA’s 510(k) premarket notification process and comply with Unique Device Identification (UDI) requirements. This means their products are listed in the FDA’s regulatory databases, including the 510(k) and UDI registries.

Recovery Force, LLC’s devices fall under FDA Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness. Since these devices are not invasive but are intended for therapeutic use (e.g., improving venous return), they require validation through the 510(k) process to demonstrate compliance with regulatory standards.

Recovery Force, LLC’s devices are listed in the FDA’s 510(k) Premarket Notification Database and the FDA’s Unique Device Identifier (UDI) System. These registries track authorised medical devices in the US, ensuring transparency and compliance with FDA requirements for devices like intermittent venous compression systems.