Aesculap, Inc. - FDA 510(k) Cleared Devices
207
Total
201
Cleared
0
Denied
FDA 510(k) cleared devices by Aesculap, Inc. Neurology ✕
60 devices
Cleared
Dec 16, 2024
XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
Neurology
160d
Cleared
Jun 29, 2023
SQ.line KERRISON
Neurology
209d
Cleared
Dec 13, 2021
Aesculap Slim Clip Applier
Neurology
206d
Cleared
Aug 24, 2021
ELAN 4 Electro Motor System
Neurology
245d
Cleared
Jan 21, 2021
DIR 800
Neurology
153d
Cleared
May 08, 2020
Ventricular Catheter
Neurology
29d
Cleared
Nov 21, 2019
M. Blue Adjustable Shunt System
Neurology
92d
Cleared
Aug 09, 2019
ELAN 4 Tools
Neurology
263d
Cleared
Jul 05, 2019
Miethke Shunt System GAV 2.0 and SA 2.0 Valves
Neurology
154d
Cleared
Jan 19, 2019
ELAN 4 Tools
Neurology
127d
Cleared
Nov 09, 2018
ELAN 4 Air Motor System
Neurology
410d
Cleared
Oct 17, 2018
ELAN 4 Electro Motor System Tools
Neurology
404d
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