Aktormed GmbH - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Aktormed GmbH has 4 FDA 510(k) cleared medical devices. Based in Barbing, DE.
Latest FDA clearance: Aug 2024. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aktormed GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Aktormed GmbH
4 devices
Cleared
Aug 08, 2024
SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499)
General & Plastic Surgery
314d
Cleared
Apr 25, 2024
ENDOFIX EXO
General & Plastic Surgery
259d
Cleared
Dec 22, 2020
SoloAsisst II, Voice Control
General & Plastic Surgery
300d
Cleared
Sep 21, 2018
SOLOASSIST II
General & Plastic Surgery
449d