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Neuravi, Ltd.

FDA Regulatory Profile

Neuravi, Ltd. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Sep 25, 2025

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K251789EMBOTRAP III Revascularization DeviceSep 25, 2025
K233924EMBOGUARD Balloon Guide CatheterApr 18, 2024
K212340EMBOGUARD Balloon Guide CatheterDec 17, 2021
K212908EmboTrap II Revascularization Device, EMBOTRAP III Revascularization DeviceOct 13, 2021
K211338EMBOTRAP III Revascularization DeviceJul 30, 2021
K193063EMBOTRAP III Revascularization DeviceJul 14, 2020
K173452EmboTrap ll Revascularization DeviceMay 9, 2018

FDA data resources