Piraeus Medical, Inc. is one of 26057 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Piraeus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 70 NeuGlide Catheter, 35 Helix Guidewire
2
Total
2
Cleared
0
Denied
Piraeus Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Maple Grove, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Piraeus Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Piraeus Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Piraeus Medical, Inc.
2 devices