Data / Medical devices / Catheter, Intravascular, Diagnostic / Ireland
FDA-registered makers of Catheter, Intravascular, Diagnostic in Ireland: 5 establishments
5 establishments in Ireland are registered with the FDA to make Catheter, Intravascular, Diagnostic (product code DQO). 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
- Catheter, Intravascular, Diagnostic
- Product code
- DQO
- Country
- Ireland
Makers of Catheter, Intravascular, Diagnostic in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Boston Scientific Limited | GALWAY Galway(County), Ireland | Manufacturer | 5 | October 29, 2015 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Limited | CORK Munster, Ireland | Manufacturer | 3 | November 26, 2002 | 0 | 0 | 0 | api.fda.gov |
| Phenox Limited | Galway Galway(County), Ireland | Manufacturer | 2 | November 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Arrotek Medical Ltd | Co. Sligo Connaught, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EPIC MedTec OEM Ireland Limited | ANNACOTTY Limerick(County), Ireland | 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.