Scopis GmbH is one of 467 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Scopis GmbH - FDA 510(k) Cleared Devices
Recent clearances: Scopis Extended Instrument Set EM, Scopis Hybrid Navigation System EM
2
Total
2
Cleared
0
Denied
Scopis GmbH has 2 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Scopis GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Phiama, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Scopis GmbH
2 devices