Endovascular Engineering

FDA Regulatory Profile

Endovascular Engineering appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 3, 2026.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261800Helo Max Thrombectomy System (HEL2090)September 3, 2026
K252956Helo Thrombectomy SystemDecember 18, 2025
K223891Cobra Catheter SystemFebruary 15, 2023