Cerenovus, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) cleared devices by Cerenovus, Inc. Neurology ✕
8 devices
Cleared
Aug 22, 2025
CEREGLIDE 71 Catheter System
Neurology
70d
Cleared
Oct 16, 2024
CEREGLIDE 42 Intermediate Catheter
Neurology
168d
Cleared
Oct 16, 2024
CEREGLIDE 42 Intermediate Catheter
Neurology
167d
Cleared
May 09, 2024
CEREGLIDE 92 Catheter System
Neurology
143d
Cleared
Jan 17, 2024
Cerenovus Large Bore Catheter
Neurology
30d
Cleared
Nov 29, 2023
CEREGLIDE 92 Intermediate Catheter
Neurology
258d
Cleared
Mar 09, 2023
CEREGLIDE 71 Intermediate Catheter
Neurology
251d
Cleared
Mar 09, 2023
CEREGLIDE 71 Intermediate Catheter
Neurology
251d