Vitrolife A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Vitrolife A/S - FDA 510(k) Cleared Devices
Recent clearances: EmbryoSlide+ ic8 dish, KIDScore D3, EmbryoScope+
4
Total
4
Cleared
0
Denied
Vitrolife A/S has 4 FDA 510(k) cleared medical devices. Based in Viby J, DK.
Last cleared in 2022. Active since 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vitrolife A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vitrolife A/S
4 devices