Vivonic GmbH is one of 208 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vivonic GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Vivonic GmbH has 2 FDA 510(k) cleared medical devices. Based in Sailauf, DE.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vivonic GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vivonic GmbH
2 devices