Adeor Medical AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Adeor Medical AG - FDA 510(k) Cleared Devices
Recent clearances: Velocity Alpha MR High Speed Surgical Drill System, Velocity Alpha Highspeed Surgical Drill System, Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical nxt Single-Use Non-stick Bipolar Forceps
4
Total
4
Cleared
0
Denied
Adeor Medical AG has 4 FDA 510(k) cleared medical devices. Based in Valley, DE.
Latest FDA clearance: Mar 2026. Active since 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Adeor Medical AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jalex Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Adeor Medical AG
4 devices
Cleared
Mar 06, 2026
Velocity Alpha MR High Speed Surgical Drill System
Neurology
100d
Cleared
Apr 11, 2021
Velocity Alpha Highspeed Surgical Drill System
Neurology
677d
Cleared
May 22, 2020
Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical nxt Single-Use...
General & Plastic Surgery
317d
Cleared
Jun 27, 2014
HICUT HIGHSPEED INSTRUMENT
Neurology
465d