Data / Medical devices / Tubes, Vials, Systems, Serum Separators, Blood Collection / Mexico
FDA-registered makers of Tubes, Vials, Systems, Serum Separators, Blood Collection in Mexico: 8 establishments
8 establishments in Mexico are registered with the FDA to make Tubes, Vials, Systems, Serum Separators, Blood Collection (product code JKA). 5 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
- Tubes, Vials, Systems, Serum Separators, Blood Collection
- Product code
- JKA
- Country
- Mexico
Makers of Tubes, Vials, Systems, Serum Separators, Blood Collection in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ICU Medical Healthcare Manufacturing S.A. de C.V. | Tijuana, B.C. C.P. Baja California, Mexico | Manufacturer | 2 | July 21, 2008 | 0 | 0 | 0 | api.fda.gov |
| Westmed Javid de Mexico, S.A. de C.V. | NOGALES Sonora, Mexico | Manufacturer | 2 | April 14, 1995 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 1 | August 12, 1992 | 0 | 0 | 0 | api.fda.gov |
| Life Outcomes Javid de Mexico | Nogales Sonora, Mexico | Manufacturer, Repackager or relabeler | 1 | January 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medline Industries, LP - Mexicali (MXC) | Mexicali Baja California, Mexico | Manufacturer | 1 | August 30, 1996 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson De Mexico | CUAUTITLAN, IZCALLI Queretaro, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. S.A. de C.V. | NOGALES Sonora, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coastline de Mexico SA de CV | Tijuana Baja California, 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.