Data / Medical devices / Mexico / Cordis de Mexico SA de CV
Cordis de Mexico SA de CV: FDA-registered device maker in Ciudad Juarez, Chihuahua Mexico, Mexico, 38 510(k) clearances
Cordis de Mexico SA de CV is registered with the FDA (registration 3008264254) in Ciudad Juarez, Chihuahua Mexico, Mexico. It lists 8 device types. The FDA files 38 510(k) clearances under its listings, the newest dated August 13, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3008264254
- Address
- Calle Circuito Interior Norte #1820 Parque Industrial Salvarcar, Ciudad Juarez, Chihuahua Mexico, Mexico, C.P. 32574
- Owner or operator
- Cerenovus, Inc. (9026915)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer
- First device listed
- October 23, 2008
- Registered through
- 2027
- Brand names listed
- CEREBASE DA Guide Sheath, CEREGLIDE 42 Intermediate Catheter, CEREGLIDE 57 Intermediate Catheter, CEREGLIDE 71 Catheter System, CEREGLIDE 71 Intermediate Catheter, CEREGLIDE 92 Catheter System, CEREGLIDE 92 Intermediate Catheter, CERENOVUS Aspiration Tubing Set and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Continuous Flush | KRA | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Diagnostic | DQO | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous | DQY | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Percutaneous, Neurovasculature | QJP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Catheter, Thrombus Retriever | NRY | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Device, Neurovascular Embolization | HCG | 2 | Manufacturer | accessdata.fda.gov |
| Device, Vascular, For Promoting Embolization | KRD | 2 | Manufacturer | accessdata.fda.gov |
| Wire, Guide, Catheter | DQX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 13, 2026 | K262398 | CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set | NRY | Substantially Equivalent | CERENOVUS, Inc. | accessdata.fda.gov |
| August 22, 2025 | K251828 | CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set | NRY | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| October 16, 2024 | K241244 | CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter | QJP | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| October 16, 2024 | K241221 | CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set | NRY | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| May 9, 2024 | K233982 | CEREGLIDE 92 Catheter System | QJP | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| April 18, 2024 | K233924 | EMBOGUARD Balloon Guide Catheter | QJP | Substantially Equivalent | Neuravi Limited | accessdata.fda.gov |
| November 29, 2023 | K230726 | CEREGLIDE 92 Intermediate Catheter | QJP | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| March 9, 2023 | K221934 | CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set | NRY | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| March 9, 2023 | K221930 | CEREGLIDE 71 Intermediate Catheter | QJP | Substantially Equivalent | Cerenovus, Inc. | accessdata.fda.gov |
| July 14, 2022 | K220040 | CEREPAK Uniform, Uniform XL, Uniform 3D, Heliform Soft, Heliform XtraSoft, Heliform XL, Heliform XtraSoft XL, Freeform, Freeform Mini, and Freeform XtraSoft Detachable Coil Systems | HCG | Substantially Equivalent | Medos International SARL | accessdata.fda.gov |
| April 12, 2022 | K214025 | PROWLER SELECT LP ES Microcatheter; PROWLER XS Microcatheter | KRA | Substantially Equivalent | Medos International SARL | accessdata.fda.gov |
| December 17, 2021 | K212340 | EMBOGUARD Balloon Guide Catheter | QJP | Substantially Equivalent | Neuravi Limited | accessdata.fda.gov |
| August 25, 2021 | K210838 | PROWLER SELECT PLUS; PROWLER EX | KRA | Substantially Equivalent | Medos International SARL | accessdata.fda.gov |
| July 30, 2021 | K211338 | EMBOTRAP III Revascularization Device | NRY | Substantially Equivalent | Neuravi, Ltd. | accessdata.fda.gov |
| July 20, 2020 | K193380 | CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set | NRY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| July 14, 2020 | K193063 | EMBOTRAP III Revascularization Device | NRY | Substantially Equivalent | Neuravi, Ltd. | accessdata.fda.gov |
| February 27, 2020 | K192804 | CEREBASE DA Guide Sheath, 95cm, CEREBASE DA Guide Sheath, 90cm, CEREBASE DA Guide Sheath, 80cm, CEREBASE DA Guide Sheath, 70cm | QJP | Substantially Equivalent | Medos International SARL | accessdata.fda.gov |
| November 8, 2019 | K191237 | CERENOVUS Large Bore Catheter | DQY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| May 9, 2018 | K173452 | EmboTrap ll Revascularization Device | NRY | Substantially Equivalent | Neuravi, Ltd. | accessdata.fda.gov |
| April 24, 2014 | K140080 | ENVOY DISTAL ACCESS (DA) GUIDING CATHETER, 6F, 95CM & 105CM, STRAIGHT & XB, MPD & XB, MPC & XB | DQY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| April 21, 2014 | K140307 | ENVOY GUIDING CATHETER | DQY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| February 24, 2012 | K120229 | ENVOY DISTAL ACCESS GUIDING CATHETER | DQY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| May 26, 2010 | K093973 | TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM | HCG | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| November 6, 2009 | K093184 | ENVOY GUIDING CATHETERS | DQY | Substantially Equivalent | Codman & Shurtleff, Inc. | accessdata.fda.gov |
| May 2, 2008 | K080967 | TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS SYRINGE II, ALSO KNOWN AS THE TRUFILL DCS ORBIT | HCG | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| September 26, 2007 | K071962 | VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER) | HCG | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| May 22, 2002 | K021591 | PROWLER SELECT (10, 14, AND PLUS) INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| March 7, 2002 | K014041 | TRUFILL DCS DETACHABLE COIL AND FRUFILL DCS SYRINGE, ALSO KNOWN AS THE TRUFILL DCS DETACHABLE COIL SYSTEM | HCG | Substantially Equivalent | Cordis Neurovascular | accessdata.fda.gov |
| January 8, 2001 | K003925 | PROWLER INFUSION CATHETERS WITH PRE-SHAPED TIPS | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| October 28, 1999 | K993266 | PROWLER PLUS INFUSION CATHETER | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| March 24, 1999 | K983483 | VASCULAR OCCLUSION SYSTEM | HCG | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| November 4, 1997 | K972518 | TRANSIT/RAPIDTRANSIT/SPEEDSTER/PROWLER INFUSION CATHETER | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| March 11, 1996 | K955637 | ESSENCE GUIDEWIRE | DQX | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| December 22, 1995 | K954949 | TRANSIT INFUSION CATHETER WITH SIDEHOLES | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| August 21, 1995 | K952874 | TRANSIT INFUSION CATHETER | KRA | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| August 8, 1995 | K950910 | TRANSIT-2 INFUSION CATHETER | DQO | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| July 18, 1994 | K936282 | TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) | DQO | Substantially Equivalent | Cordis Neurovascular, Inc. | accessdata.fda.gov |
| May 31, 1994 | K936260 | TRANSIT INFUSION CATHETER | DQO | Substantially Equivalent | Cordis Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Neurovascular Embolization
- All makers of Catheter, Percutaneous, Neurovasculature
- All makers of Catheter, Continuous Flush
- All makers of Catheter, Thrombus Retriever
- All makers of Catheter, Percutaneous
- All makers of Device, Vascular, For Promoting Embolization
Updated August 13, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.