Hamilton Medical AG - FDA 510(k) Cleared Devices

Hamilton Medical AG, is a manufacturer of mechanical ventilation systems and respiratory care devices with a manufacturing facility in Reno, US. The company develops ventilators, oxygen therapy devices, and integrated accessories for critical care, emergency transport, and anesthesia applications.

Hamilton Medical has received 30 FDA 510(k) clearances from 30 total submissions. The company specializes exclusively in Anesthesiology devices. FDA 510(k) clearances span from 2003 to 2021, establishing a strong regulatory track record over nearly two decades.

Notable cleared devices include the HAMILTON-C3, HAMILTON-C6, HAMILTON-G5, HAMILTON-T1, HAMILTON-H900, and IntelliCuff systems. The company is recognized for intelligent ventilation technologies and microprocessor-based respiratory solutions designed for diverse clinical environments.

This company profile reflects historical FDA 510(k) regulatory activity. For detailed device names, product codes, and clearance dates, explore the complete submission record.