Datex-Ohmeda, Inc. - FDA 510(k) Cleared Devices
60
Total
60
Cleared
0
Denied
Datex-Ohmeda, Inc. has 60 FDA 510(k) cleared anesthesiology devices. Based in Madison, US.
Latest FDA clearance: Oct 2025. Active since 1998.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Datex-Ohmeda, Inc.
60 devices
Cleared
Oct 22, 2025
Giraffe OmniBed Carestation (CS1)
General Hospital
145d
Cleared
Mar 28, 2023
Carestation 750/750c
Anesthesiology
473d
Cleared
Mar 02, 2022
Giraffe Omnibed Carestation CS1
General Hospital
114d
Cleared
Mar 02, 2022
Giraffe Incubator Carestation CS1
General Hospital
114d
Cleared
Nov 04, 2021
CARESCAPE R860
Anesthesiology
268d
Cleared
Jan 04, 2018
Tec 820, Tec 850
Anesthesiology
119d
Cleared
Nov 03, 2017
Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100,...
Anesthesiology
120d
Cleared
Aug 15, 2017
Aisys CS2
Anesthesiology
145d
Cleared
Jan 21, 2016
Carestation 620/650/650C
Anesthesiology
225d
Cleared
Jun 12, 2015
CARESCAPE R860
Anesthesiology
266d
Cleared
Apr 24, 2015
Aespire View
Anesthesiology
133d
Cleared
Feb 03, 2015
ENGSTROM CARESTATION, ENGSTROM PRO
Anesthesiology
334d
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