Aevumed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K254306Aevumed FENIX Suture AnchorMarch 4, 2026
K260004Aevumed PROTEKT Suture AnchorJanuary 28, 2026
K253040Aevumed FASE Suture AnchorOctober 21, 2025
K242895Aevumed PHANTOM Suture AnchorsAugust 6, 2025
K223878Aevumed RAPID Suture AnchorsMarch 17, 2023
K222363Aevumed PHANTOM™-LP Suture AnchorsNovember 28, 2022
K180464AEVUMED PHANTOM Suture AnchorsMay 31, 2018