ClearanceBrief
Company ยท IE

Perfuze, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (3 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NRYCatheter, Thrombus Retriever6
QJPCatheter, Percutaneous, Neurovasculature5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 12, 2026K262399Millipede System
Perfuze, Ltd., IE
NRY
Jul 9, 2026K253901Millipede88 Access Catheter
Perfuze, Ltd., IE
QJP
Mar 16, 2026K253590Millipede System
Perfuze, Ltd., IE
NRY
Aug 29, 2025K252392Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set
Perfuze, Ltd., IE
NRY
Feb 26, 2025K250012Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
Perfuze, Ltd., IE
NRY
Oct 17, 2024K240711Zipline Access Catheter
Perfuze, Ltd., IE
QJP
Sep 20, 2024K242504Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
Perfuze, Ltd., IE
NRY
Dec 14, 2023K233648Millipede 088 Access Catheter
Perfuze, Ltd., IE
QJP
Oct 18, 2023K232524Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
Perfuze, Ltd., IE
NRY
Sep 19, 2023K231802Millipede 088 Access Catheter
Perfuze, Ltd., IE
QJP
Sep 20, 2022K214048Millipede 088 Access Catheter
Perfuze, Ltd., IE
QJP

Latest recalls

DateFirm and productCodeLinked 510(k)
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