Siemens Corp. - FDA 510(k) Cleared Devices

Siemens Corp., is a global technology company headquartered in McHenry, US. The company develops medical imaging and diagnostic equipment for healthcare providers worldwide.

Siemens has received 66 FDA 510(k) clearances from 66 total submissions. The company's regulatory focus centers on Radiology devices, which represent the dominant category of its cleared portfolio. FDA 510(k) clearances span from 1978 to 2010, establishing a significant historical record in medical device regulation.

Recent cleared devices include advanced imaging systems such as CT scanners, MR systems, X-ray tables, and specialized software packages for diagnostic imaging. The company's portfolio reflects expertise in computed tomography, magnetic resonance imaging, nuclear medicine, and interventional radiology technologies.

This company profile is maintained as a historical regulatory record. Explore the complete list of device names, product codes, and individual clearance dates in the database.