Syntheticmr AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Syntheticmr AB has 6 FDA 510(k) cleared medical devices. Based in Linkoping, SE.
Last cleared in 2021. Active since 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Syntheticmr AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Syntheticmr AB
6 devices