Data / Medical devices / Set, Administration, Intravascular / Costa Rica
FDA-registered makers of Set, Administration, Intravascular in Costa Rica: 5 establishments
5 establishments in Costa Rica are registered with the FDA to make Set, Administration, Intravascular (product code FPA). 3 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
- Set, Administration, Intravascular
- Product code
- FPA
- Country
- Costa Rica
Makers of Set, Administration, Intravascular in Costa Rica
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Baxter Productos Medicos, Ltda. | 1-7052 Cartago, Costa Rica | Manufacturer | 18 | March 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Costa Rica Ltd. | La Aurora de Heredia, Costa Rica | Manufacturer | 14 | January 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| Allergan | La Aurora De Heredia, Costa Rica | Manufacturer | 1 | July 14, 1995 | 0 | 0 | 0 | api.fda.gov |
| Biomerics Alajuela | Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerics Cartago | Cartago, Costa Rica | 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.