Data / Medical devices / Catheter, Percutaneous / Ireland
FDA-registered makers of Catheter, Percutaneous in Ireland: 10 establishments
10 establishments in Ireland are registered with the FDA to make Catheter, Percutaneous (product code DQY). 6 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
- Catheter, Percutaneous
- Product code
- DQY
- Country
- Ireland
Makers of Catheter, Percutaneous in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medtronic Ireland | GALWAY Galway(County), Ireland | Manufacturer | 15 | October 29, 2025 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Limited | GALWAY Galway(County), Ireland | Manufacturer | 13 | February 1, 2024 | 0 | 0 | 0 | api.fda.gov |
| Stryker Neurovascular | Cork Munster, Ireland | Manufacturer | 8 | March 13, 2019 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Limited | CORK Munster, Ireland | Manufacturer | 1 | March 15, 2019 | 0 | 0 | 0 | api.fda.gov |
| Creagh Medical Ltd. | Co. Galway Galway(County), Ireland | Complaint file establishment, Manufacturer | 1 | January 12, 2018 | 0 | 0 | 0 | api.fda.gov |
| Marvao Medical Devices Ltd. | Galway Galway(County), Ireland | Complaint file establishment, Specification developer | 1 | June 2, 2022 | 0 | 0 | 0 | api.fda.gov |
| Abbott Vascular | CLONMEL Tipperary, Ireland | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arrotek Medical Ltd | Co. Sligo Connaught, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clearstream Technologies Ltd. | Wexford, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lake Region Medical Limited | NEW ROSS Wexford, Ireland | 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.