Data / Medical devices / Tube, Tracheal (W/Wo Connector) / Mexico
FDA-registered makers of Tube, Tracheal (W/Wo Connector) in Mexico: 9 establishments
9 establishments in Mexico are registered with the FDA to make Tube, Tracheal (W/Wo Connector) (product code BTR). 6 have 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
- Tube, Tracheal (W/Wo Connector)
- Product code
- BTR
- Country
- Mexico
Makers of Tube, Tracheal (W/Wo Connector) in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Teleflex Medical de Tecate, S. de R.L de C.V. | TECATE Baja California, Mexico | Manufacturer, Repackager or relabeler | 15 | November 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Ciudad Juarez Chihuahua, Mexico | Contract manufacturer, Manufacturer | 9 | May 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | Tijuana, B.C. C.P. Baja California, Mexico | Manufacturer | 6 | August 13, 2008 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 2 | March 8, 1983 | 0 | 0 | 0 | api.fda.gov |
| AVENT S. de R.L. de C.V. | NOGALES Sonora, Mexico | Manufacturer | 1 | May 11, 2012 | 0 | 0 | 0 | api.fda.gov |
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer, Manufacturer | 1 | January 6, 1993 | 0 | 0 | 0 | api.fda.gov |
| Integra Biotechnical, SA de CV | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laboratorios PiSA, S. A. de C.V. | Tlajomulco de Zuniga Jalisco, Mexico | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical de Mexico, S. de R.L. de C.V. | NUEVO LAREDO Tamaulipas, 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.