UPlanner B.V. - Presurgeo is one of 118 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
UPlanner B.V. - Presurgeo - FDA 510(k) Cleared Devices
Recent clearances: SkeletonPlanner
1
Total
1
Cleared
0
Denied
UPlanner B.V. - Presurgeo has 1 FDA 510(k) cleared medical devices. Based in Vreeland, NL.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by UPlanner B.V. - Presurgeo Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Britton Medical Consultancy, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - UPlanner B.V. - Presurgeo
1 devices