Go-Pen Aps is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Go-Pen Aps - FDA 510(k) Cleared Devices
Recent clearances: GO-PEN®
1
Total
1
Cleared
0
Denied
Go-Pen Aps has 1 FDA 510(k) cleared medical devices. Based in Kongens Lyngby, DK.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Go-Pen Aps Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Veranex as regulatory consultant.
FDA 510(k) Regulatory Record - Go-Pen Aps
1 devices