Data / Medical devices / Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass / Mexico
FDA-registered makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass in Mexico: 7 establishments
7 establishments in Mexico are registered with the FDA to make Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass (product code DTL). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- Product code
- DTL
- Country
- Mexico
Makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medtronic Mexico S. de R.L. de CV | Tijuana Baja California, Mexico | Manufacturer | 6 | August 15, 1990 | 0 | 0 | 0 | api.fda.gov |
| Tri-State De Mexico, S. De R.L. De C.V. | MEXICALI Baja California, Mexico | Manufacturer | 2 | January 12, 1989 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 1 | September 11, 1991 | 0 | 0 | 0 | api.fda.gov |
| Productos Medline S.A. De C.V. | NUEVO LAREDO Tamaulipas, Mexico | Manufacturer, Repackager or relabeler | 1 | January 23, 1979 | 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 | |
| Merit Maquiladora Mexico, S. DE R.L. DE C.V. | Tijuana Baja California, Mexico | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical de Tecate, S. de R.L de C.V. | TECATE Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.