Shenzhen Future Electronic Co., Ltd.

Shenzhen Future Electronic Co., Ltd. specializes in two primary categories of medical devices: reusable multi-chamber venous compression system garments and transcutaneous neuromuscular electrical stimulation (TENS) systems for physical therapy. Their product line includes standalone TENS units, such as the ST-304 model, and air compression therapy devices, including models like the ST-502, ST-504, ST-505, ST-506, and ST-507. These devices are designed to support venous circulation and muscle recovery through sequential pneumatic compression or electrical stimulation.

Shenzhen Future Electronic Co., Ltd. is based in the United States. While the company name includes 'Shenzhen,' its operational headquarters and regulatory presence are established within the U.S., where its devices are developed, manufactured, and distributed.

Devices manufactured by Shenzhen Future Electronic Co., Ltd. are recorded in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries track Class II devices like their TENS systems and air compression therapy devices to ensure compliance with U.S. regulatory requirements.

The devices produced by Shenzhen Future Electronic Co., Ltd., such as their transcutaneous electrical nerve stimulators and air compression therapy systems, are classified as Class II under FDA regulations. This classification applies to devices that pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure safety and effectiveness without requiring the stringent pre-market approval process of Class III devices.