Perfuze, Ltd.
Perfuze, Ltd. appears in FDA public data with 0 recalls, 10 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 9, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253901 | Millipede88 Access Catheter | July 9, 2026 |
| K253590 | Millipede System | March 16, 2026 |
| K252392 | Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set | August 29, 2025 |
| K250012 | Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set | February 26, 2025 |
| K240711 | Zipline Access Catheter | October 17, 2024 |
| K242504 | Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set | September 20, 2024 |
| K233648 | Millipede 088 Access Catheter | December 14, 2023 |
| K232524 | Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set | October 18, 2023 |
| K231802 | Millipede 088 Access Catheter | September 19, 2023 |
| K214048 | Millipede 088 Access Catheter | September 20, 2022 |