Neuravi Limited

FDA Regulatory Profile

Neuravi Limited appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 25, 2025.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251789EMBOTRAP III Revascularization DeviceSeptember 25, 2025
K233924EMBOGUARD Balloon Guide CatheterApril 18, 2024
K212340EMBOGUARD Balloon Guide CatheterDecember 17, 2021