Vitrolife GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vitrolife GmbH - FDA 510(k) Cleared Devices
Recent clearances: LaserShot M, NaviLase
1
Total
1
Cleared
0
Denied
Vitrolife GmbH has 1 FDA 510(k) cleared medical devices. Based in Bruckberg, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vitrolife GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vitrolife GmbH
1 devices