Company ยท IE
Neuravi, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2025. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 25, 2025 | K251789 | EMBOTRAP III Revascularization Device Neuravi Limited, IE | NRY |
| Apr 18, 2024 | K233924 | EMBOGUARD Balloon Guide Catheter Neuravi Limited, IE | QJP |
| Dec 17, 2021 | K212340 | EMBOGUARD Balloon Guide Catheter Neuravi Limited, IE | QJP |
| Oct 13, 2021 | K212908 | EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device Neuravi, Ltd., IE | NRY |
| Jul 30, 2021 | K211338 | EMBOTRAP III Revascularization Device Neuravi, Ltd., IE | NRY |
| Jul 14, 2020 | K193063 | EMBOTRAP III Revascularization Device Neuravi, Ltd., IE | NRY |
| May 9, 2018 | K173452 | EmboTrap ll Revascularization Device Neuravi, Ltd., IE | NRY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||