Aevumed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Aevumed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Malvern, US.
Latest FDA clearance: Mar 2026. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Aevumed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Aevumed, Inc.
7 devices
Cleared
Mar 04, 2026
Aevumed FENIX Suture Anchor
Orthopedic
63d
Cleared
Jan 28, 2026
Aevumed PROTEKT Suture Anchor
Orthopedic
26d
Cleared
Oct 21, 2025
Aevumed FASE Suture Anchor
Orthopedic
29d
Cleared
Aug 06, 2025
Aevumed PHANTOM Suture Anchors
Orthopedic
317d
Cleared
Mar 17, 2023
Aevumed RAPID Suture Anchors
Orthopedic
80d
Cleared
Nov 28, 2022
Aevumed PHANTOM™-LP Suture Anchors
Orthopedic
116d
Cleared
May 31, 2018
AEVUMED PHANTOM Suture Anchors
Orthopedic
99d