ClearanceBrief
Company ยท DE

Inomed Medizintechnik GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 2026. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ETNStimulator, Nerve5
GWFStimulator, Electrical, Evoked Response4
GWQFull-Montage Standard Electroencephalograph1
GZLElectrode, Depth1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 24, 2026K263010ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress
inomed Medizintechnik GmbH, DE
GWF
Jun 13, 2025K242852ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM T
Inomed Medizintechnik GmbH, DE
ETN
Oct 27, 2023K233292ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress
Inomed Medizintechnik GmbH, DE
GWF
Jan 27, 2023K223254C2 Xplore
Inomed Medizintechnik GmbH, DE
ETN
Nov 11, 2022K212164Mapping Suction Probe
Inomed Medizintechnik GmbH, DE
ETN
Jan 7, 2022K212166ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress
Inomed Medizintechnik GmbH, DE
GWF
Feb 1, 2016K152505C2 NerveMonitor System
Inomed Medizintechnik GmbH, DE
ETN
Oct 6, 2011K111647C2 NERVEMONITOR SYSTEM WITH ACCESSORIES
Inomed Medizintechnik GmbH, DE
GWF
Nov 18, 2009K091874INOMED ADHESIVE LARYNGEAL ELECTRODES, MODELS 530655, 530656
Inomed Medizintechnik GmbH
ETN
Mar 18, 2005K042208ISIS MER SYSTEM/ELEKTA MER SYSTEM
Inomed Medizintechnik GmbH, DE
GZL
Oct 2, 1991K910972WALTER GRAPHTEK
Inomed Medizintechnik GmbH, DE
GWQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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