Medical Device Manufacturer · DK , Viby J

Vitrolife A/S - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2015

Total

Cleared

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) cleared devices by Vitrolife A/S

4 devices

1-4 of 4