Medical Device Manufacturer · NL , Kerkrade

Technomed Europe - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1999

Recent clearances: MR Conditional Cup Electrodes, Disposable Concentric Needle Electrode 0.30x25mm Red (TE/B50700-001), Disposable Subdermal Needle Electrode, Corkscrew

13
Total
13
Cleared
0
Denied

Technomed Europe has 13 FDA 510(k) cleared neurology devices. Based in Kerkrade, NL.

Latest FDA clearance: May 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) Regulatory Record - Technomed Europe

13 devices
1-13 of 13
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