De G?tzen S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
De G?tzen S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology), X-MIND prime (under trade mark Acteon), I-MAX (under trade mark Owandy Radiology)
2
Total
2
Cleared
0
Denied
De G?tzen S.R.L. has 2 FDA 510(k) cleared medical devices. Based in Olgiate Olona, IT.
Last cleared in 2023. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by De G?tzen S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by De Götzen S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - De G?tzen S.R.L.
2 devices