Anutra Medical, Inc.

Anutra Medical, Inc. specializes in single-use general-purpose syringes, with a focus on medical aspiration procedures. Their most common product is the ANUTRA Feedback Aspiration Syringe, which includes feedback mechanisms to enhance precision during fluid extraction. These devices are designed for controlled and accurate medical applications.

Anutra Medical, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance, manufacturing standards, and distribution networks within the region.

Anutra Medical’s devices, including their general-purpose syringes like the ANUTRA Feedback Aspiration Syringe, are classified as Class II medical devices by the FDA. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

Anutra Medical’s devices are included in the FDA’s 510(k) Premarket Notification database, which tracks medical devices deemed substantially equivalent to legally marketed predicates. Additionally, their products appear in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and identification in the healthcare supply chain. These listings help healthcare providers and regulators verify compliance and device details.