Data / Medical devices / Catheter, Thrombus Retriever / Ireland
FDA-registered makers of Catheter, Thrombus Retriever in Ireland: 5 establishments
5 establishments in Ireland are registered with the FDA to make Catheter, Thrombus Retriever (product code NRY). 4 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, Thrombus Retriever
- Product code
- NRY
- Country
- Ireland
Makers of Catheter, Thrombus Retriever in Ireland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Perfuze | Dangan Galway(County), Ireland | Manufacturer | 6 | August 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Neuravi Limited | Galway Galway(County), Ireland | Specification developer | 4 | September 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Stryker Neurovascular | Cork Munster, Ireland | Manufacturer | 2 | March 13, 2019 | 0 | 0 | 0 | api.fda.gov |
| Phenox Limited | Galway Galway(County), Ireland | Complaint file establishment, Manufacturer | 1 | January 15, 2026 | 0 | 0 | 0 | api.fda.gov |
| Advant Medical Ltd | BallyBrit Galway(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.