Data / Medical devices / Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter / Mexico
FDA-registered makers of Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter in Mexico: 8 establishments
8 establishments in Mexico are registered with the FDA to make Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter (product code OAD). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
- Product code
- OAD
- Country
- Mexico
Makers of Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cordis de Mexico, SA de CV | JUAREZ Chihuahua, Mexico | Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Amphenol Alden Products Company | Hermosillo Sonora, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| AvailMed S.A.De C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foxconn Baja California S.A De C.V. | tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Molex S.A. De C.V. | Nogales Sonora, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NPA de Mexico S.de R.L. de C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Plexus Electronica S. de R.L. de C.V.. | Zapopan Jalisco, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Venusa de Mexico S. de R.L de C.V | CIUDAD JUAREZ Chihuahua, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.