Disa Medinotec

FDA Regulatory Profile

Disa Medinotec appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 11, 2025.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241562OutFlo Aortic Valve Dilatation Balloon CatheterMarch 11, 2025
K211894TrachealatorNovember 24, 2021