Technomed Europe - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Technomed Europe has 12 FDA 510(k) cleared neurology devices. Based in Kerkrade, NL.
Latest FDA clearance: Mar 2026. Active since 1999.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Technomed Europe
12 devices
Cleared
Mar 15, 2026
Disposable Concentric Needle Electrode 0.30x25mm Red (TE/B50700-001)
Neurology
118d
Cleared
Dec 11, 2024
Disposable Subdermal Needle Electrode, Corkscrew
Neurology
238d
Cleared
Jul 19, 2013
DISPOSABLE AND REUSABLE CONCENTRIC NEEDLE ELECTRODES,DISPOSABLE AND REUSABLE...
Neurology
182d
Cleared
Aug 28, 2012
LARYNGEAL ELECTRODE
Ear, Nose, Throat
124d
Cleared
May 26, 2011
SURGICAL STIMULATORS
Ear, Nose, Throat
101d
Cleared
May 01, 2008
DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES
Neurology
136d
Cleared
Oct 19, 2007
CUP ELECTRODES, GOLD, REUSABLE, SILVER, REUSABLE
Neurology
88d
Cleared
Aug 21, 2007
DISPOSABLE PEDICLE SCREW PROBE, MODEL 3603-00
Neurology
249d
Cleared
Feb 16, 2007
DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND...
Neurology
189d
Cleared
May 05, 2005
DISPOSABLE CONCENTRIC PROBE, DISPOSABLE BIPOLAR PROBE, DISPOSABLE MONOPOLAR...
Neurology
85d
Cleared
Oct 26, 2004
SMK, CX, CXE, RCN
Neurology
55d
Cleared
May 27, 1999
ELECTRODE NEEDLES
Neurology
143d