Avinent Implant System S.L.U. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Avinent Implant System S.L.U. has 2 FDA 510(k) cleared medical devices. Based in Santpedor, ES.
Last cleared in 2021. Active since 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Avinent Implant System S.L.U. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Avinent Implant System S.L.U.
2 devices