Landauer is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Landauer - FDA 510(k) Cleared Devices
Recent clearances: Medical Radiation Dosimetry System microSTARii
1
Total
1
Cleared
0
Denied
Landauer, provides radiation monitoring services and detection devices for occupational and medical dosimetry applications. The company operates with a manufacturing facility in Glenwood, Illinois, and serves healthcare, industrial, and safety sectors globally.
Landauer has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory focus centers on Radiology devices. The Medical Radiation Dosimetry System microSTARii represents the company's cleared device portfolio. Landauer's FDA 510(k) clearance was granted in 2019.
The company is currently inactive, with no new FDA 510(k) submissions or clearances in more than five years. This profile serves as a historical regulatory record. For detailed information on device names, product codes, and clearance dates, review the complete 510(k) submission history.
FDA 510(k) Regulatory Record - Landauer
1 devices