RICO SUCTION LABS INC

Rico Suction Labs Inc. specializes in surgical suction systems. These devices are primarily used in operating rooms and medical procedures to efficiently remove fluids and debris from surgical sites, helping to improve procedural workflow and minimize contamination risks.

Rico Suction Labs Inc. is based in the United States. Its devices are regulated under U.S. FDA guidelines, where they are classified as Class II medical devices, indicating a moderate level of risk that requires specific controls to ensure safety and effectiveness.

Yes, Rico Suction Labs Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for regulatory and clinical purposes.

Rico Suction Labs Inc.’s devices fall under the FDA’s Class II classification. This classification is assigned to devices that generally pose a moderate risk to patients and require special controls beyond general controls to ensure their safety and performance, such as surgical suction systems.