Intrauma S.P.A

FDA Regulatory Profile

Intrauma S.P.A 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 Nov 12, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K252959WRISTAR MultiAx Distal Radius KitNov 12, 2025
K230623KITE Distal Fibula KitSep 1, 2023
K201147Elos® Intramedullary Nailing SystemJul 19, 2021