Cerenovus, Inc. is one of 16099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cerenovus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MICRUSFRAME (MFR100202), CEREGLIDE 57 Intermediate Catheter, CEREGLIDE 71 Catheter System
10
Total
10
Cleared
0
Denied
Cerenovus, Inc. has 10 FDA 510(k) cleared neurology devices. Based in Miami, US.
Latest FDA clearance: Aug 2026. Active since 2023.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cerenovus, Inc.
10 devices
Cleared
Aug 14, 2026
MICRUSFRAME (MFR100202)
Neurology
30d
Cleared
Aug 13, 2026
CEREGLIDE 57 Intermediate Catheter
Neurology
30d
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