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Sign in to claim this brandCerenovus, Inc.
United States·US-MF-000025013
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 6303, Waterford District Drive, Miami, FL, United States
- Website
- www.jnj.com
- —
- —
- [email protected]
- Phone
- +1 305 265 6811
- PRRC Contact
- Günter Solms
- EUDAMED SRN
- US-MF-000025013
- FDA FEI Number
- 3002947440
- DUNS Number
- 607846297
Catalogue (1435)
Page 29 of 29| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trufill Dcs Orbit | 638CS1430 | FDA UDI | Class II | Unknown |
| Codman Flex1 | 70028 | FDA UDI | Class III | Unknown |
| Cerepak Heliform | XHD100254 | FDA UDI | Class II | Active |
| Codman Hakim Bactiseal Siphonguard | NS5516 | FDA UDI | Class II | Unknown |
| Cerepak Uniform | FCX100730 | FDA UDI | Class II | Active |
| Trufill Dcs Orbit | 637HF0310 | FDA UDI | Class II | Unknown |
| Codman Hakim | 82-5493 | FDA UDI | Class II | Unknown |
| Aneuroplastic | 43-1290 | FDA UDI | Class II | Unknown |
| Codman Hakim Siphonguard Bactiseal | NS5450 | FDA UDI | Class II | Unknown |
| Codman Hakim Siphonguard | NS5023 | FDA UDI | Class II | Unknown |
| Trufill Dcs Orbit | 637CF0510 | FDA UDI | Class II | Unknown |
| Codman Hakim | NS0622 | FDA UDI | Class II | Unknown |
| Cerepak Freeform | MCR092060 | FDA UDI | Class II | Active |
| Codman Hakim | NS0388 | FDA UDI | Class II | Unknown |
| Codman Accu-Flo | 82-6101 | FDA UDI | Class II | Unknown |
| Trufill Dcs Orbit | 637CS1030 | FDA UDI | Class II | Unknown |
| Cerepak Freeform | SCR122535 | FDA UDI | Class II | Active |
| Trufill Dcs Orbit | 637HF0615 | FDA UDI | Class II | Unknown |
| Codman Hakim Rickham Bactiseal | NS5406 | FDA UDI | Class II | Unknown |
| Cerepak Freeform | SCR120515 | FDA UDI | Class II | Active |
| Codman Malis Cmc | 80-1179 | FDA UDI | Class II | Unknown |
| Codman Cerelink | 826824 | FDA UDI | Class II | Unknown |
| Codman Eds 3 | 82-1731C | FDA UDI | Class II | Unknown |
| ENPOWER detachment control box | DCB2000500 | EUDAMEDFDA UDI | Class IIa | Active |
| CEREGLIDE 92 Catheter System | K233982 | FDA 510(k) | Class II | Active |
| CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter | K241244 | FDA 510(k) | Class II | Active |
| CEREGLIDE 92 Intermediate Catheter | K230726 | FDA 510(k) | Class II | Active |
| CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set | K241221 | FDA 510(k) | Class II | Active |
| CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set | K251828 | FDA 510(k) | Class II | Active |
| CEREGLIDE 71 Intermediate Catheter | K221930 | FDA 510(k) | Class II | Active |
| CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set | K221934 | FDA 510(k) | Class II | Active |
| Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set | K233988 | FDA 510(k) | Class II | Active |
| Connecting Cable | CCB000157-00 | EUDAMEDFDA UDI | Class I | Active |
| Trufill N-Butyl Cyanoacrylate Liquid Embolic System | P990040 | FDA PMA | Class III | Active |
| ENPOWER control cable | ECB000182-00 | EUDAMEDFDA UDI | Class I | Active |
Related Companies
Authorised Representatives
Importers
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Notified Bodies
Not available yet.
Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 2, 2025 | Z-0434-2026 | — | open, classified | Detachable coils system may fail to detach, which could result in hemorrhagic and ischemic stroke, procedural delays, or the need for additional surgical intervention. |
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Cerenovus, Inc. Ciudad Juarez, Chihuahua Mexico · MX FEI 3008264254