Aspivix SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Aspivix SA - FDA 510(k) Cleared Devices
Recent clearances: Carevix™ Suction Cervical Stabilizer, ASPIVIX v1.1 Cervical Suction Tenaculum
2
Total
2
Cleared
0
Denied
Aspivix SA has 2 FDA 510(k) cleared medical devices. Based in Renens, CH.
Last cleared in 2023. Active since 2021. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Aspivix SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aspivix SA
2 devices