Pendracare is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Pendracare - FDA 510(k) Cleared Devices
Recent clearances: Primum Hydrophilic Guiding Catheter
2
Total
2
Cleared
0
Denied
Pendracare has 2 FDA 510(k) cleared medical devices. Based in Leek, NL.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pendracare Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pendracare
2 devices