Artoss GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Artoss GmbH - FDA 510(k) Cleared Devices
Recent clearances: NanoBone SBX PUTTY, NanoBone QD
3
Total
3
Cleared
0
Denied
Artoss GmbH has 3 FDA 510(k) cleared medical devices. Based in Rostock, DE.
Historical record: 3 cleared submissions from 2015 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Artoss GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Artoss GmbH
3 devices