Aevumed, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aevumed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aevumed SUPERCYNCH™ Button System, Aevumed FENIX Suture Anchor, Aevumed PROTEKT Suture Anchor
8
Total
8
Cleared
0
Denied
Aevumed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Malvern, US.
Latest FDA clearance: Sep 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.
510(k) submissions have been managed by Pyxa Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aevumed, Inc.
8 devices
Cleared
Sep 02, 2026
Aevumed SUPERCYNCH™ Button System
Orthopedic
345d
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