Cerenovus, Inc.
Cerenovus, Inc. holds FDA 510(k) medical device clearances, first cleared 2023, most recent 2026, with 1 FDA device recall on record.
Name variants for Cerenovus, Inc.
as filed with FDA- Cerenovus, Inc.
- CERENOVUS, Inc.
Top product codes for Cerenovus, Inc.
FDA recalls by Cerenovus, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Cerenovus, Inc.
- K262419 — MICRUSFRAME (19+ models)
- K262398 — CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set
- K251828 — CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set
- K241221 — CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set
- K241244 — CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
- K233982 — CEREGLIDE 92 Catheter System
- K233988 — Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set
- K230726 — CEREGLIDE 92 Intermediate Catheter
- K221930 — CEREGLIDE 71 Intermediate Catheter
- K221934 — CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set
Data sourced from openFDA. This site is unofficial and independent of the FDA.