Catheter, Thrombus Retriever
Cerenovus, Inc.'s record for this product code
MDR events134All time
Recalls0All time
510(k) clearances4All time
Recent MDR events
134 adverse event reports on file
- CEREGLIDEJul 28, 2026Malfunction3007628272-2026-00057
- CEREGLIDEJul 28, 2026Malfunction3007628272-2026-00061
- CEREGLIDEJul 16, 2026Malfunction3007628272-2026-00060
- CEREGLIDEJul 13, 2026Malfunction3007628272-2026-00058
- CEREGLIDEJul 13, 2026Malfunction3007628272-2026-00059
- CEREGLIDEJul 13, 2026Malfunction3007628272-2026-00052
- CEREGLIDEJun 25, 2026Malfunction3007628272-2026-00049
- CEREGLIDEJun 11, 2026Malfunction3007628272-2026-00044
- CEREGLIDE 57Jun 4, 2026Malfunction3007628272-2026-00045
- CEREGLIDEMay 28, 2026Injury3007628272-2026-00041
Recalls
0 recall events for this product code
No recalls on file for Cerenovus, Inc. under this product code.
510(k) clearances
4 clearances for this product code
- K251828Aug 22, 2025
CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set
- K241221Oct 16, 2024
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set
- K233988Jan 17, 2024
Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set
- K221934Mar 9, 2023
CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set