Orthokey Italia S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Orthokey Italia S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Perseus
1
Total
1
Cleared
0
Denied
Orthokey Italia S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Carrara, IT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthokey Italia S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Isemed S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Orthokey Italia S.R.L.
1 devices