ATMOS MedizinTechnik GmbH & Co. KG

ATMOS MedizinTechnik GmbH & Co. KG specializes in three primary device categories: thoracic suction pumps, endoscopic light source units (line-powered), and surgical suction pumps. These devices are developed for use in surgical and procedural environments to assist in fluid removal and illumination during minimally invasive operations.

The company is based in the United States. While the name includes 'MedizinTechnik,' which suggests a German origin, the operational headquarters and regulatory presence are established in the US.

ATMOS’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for sale in the US, ensuring traceability and compliance with regulatory requirements.

ATMOS’s devices fall into two classification tiers under FDA regulations: Class I and Class II. Class I devices generally pose minimal risk and may require fewer controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential hazards.