Perfuze, Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Perfuze, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Millipede System, Millipede70 Aspiration Catheter, Millipede 070 Aspiration Catheter
10
Total
10
Cleared
0
Denied
Perfuze, Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Galway, IE.
Latest FDA clearance: Jul 2026. Active since 2022.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Perfuze, Ltd.
10 devices
Cleared
Jul 09, 2026
Millipede88 Access Catheter
Neurology
216d
Cleared
CT
Mar 16, 2026
Millipede System
Neurology
119d
Cleared
Aug 29, 2025
Millipede70 Aspiration Catheter
Neurology
29d
Cleared
Feb 26, 2025
Millipede 070 Aspiration Catheter
Neurology
55d
Cleared
Oct 17, 2024
Zipline Access Catheter
Neurology
216d
Cleared
Sep 20, 2024
Millipede 088 Access Catheter
Neurology
29d
Cleared
Dec 14, 2023
Millipede 088 Access Catheter
Neurology
30d
Cleared
Oct 18, 2023
Millipede 070 Aspiration Catheter
Neurology
61d
Cleared
Sep 19, 2023
Millipede 088 Access Catheter
Neurology
91d
Cleared
Sep 20, 2022
Millipede 088 Access Catheter
Neurology
267d