Dosisoft SA is one of 16259 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dosisoft SA - FDA 510(k) Cleared Devices
Recent clearances: ThinkQA 3, PLANET Onco Dose (3.2), ThinkQA (Edition 2)
5
Total
5
Cleared
0
Denied
Dosisoft SA has 5 FDA 510(k) cleared medical devices. Based in Lincoln, US.
Latest FDA clearance: Jun 2026. Active since 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dosisoft SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Doslsoft SA as regulatory consultant.
FDA 510(k) Regulatory Record - Dosisoft SA
5 devices