Avinent Implant System S.L.U. is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Avinent Implant System S.L.U. - FDA 510(k) Cleared Devices
Recent clearances: Avinent Biomimetic Coral and Ocean-Iceberg Sterilization Cassettes, Avinent Surgical Tray
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