Medical Device Manufacturer · US , Indianpolis , IN

Eb Neuro S.P.A. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2001

Recent clearances: NExT Station, BE Plus PRO, Neurotravel LIGHT, STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast

Total

Cleared

Denied

Eb Neuro S.P.A. has 13 FDA 510(k) cleared neurology devices. Based in Indianpolis, US.

Latest FDA clearance: Dec 2024. Active since 2001.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Makromed, Inc., Regulatory Technology Services, LLC and Navigant Consulting, Inc..

Eb Neuro S.P.A. is one of 16052 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eb Neuro S.P.A.

13 devices

1-13 of 13

BE Plus PRO, Neurotravel LIGHT

K242305 · GWL

Neurology · 30d

Cleared Aug 19, 2015

STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast

BE PLUS LTM AMPLIFIER GWI AMPLIFIER

BE PLUS / AURA-LTM64 AMPLIFIER

SANDMAN SD20 AMPLIFIER

K040113 · GWL

Neurology · 29d

Cleared Jan 05, 2001

MIZAR, BASIS BE, SANDMAN DIGITAL

K003154 · GWL

Neurology · 87d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 09, 2026

Eb Neuro S.P.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Eb Neuro S.P.A.

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