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About NEBA®

NEBA is a biologically-based ADHD assessment aid for children and adolescents between the ages of 6 and 17. Clinicians use NEBA to detect neural activity using an EEG marker.

NEBA is quantitative and non-invasive and has been standardized for use as one part of a full psychiatric workup. Using NEBA is simple, quick, accurate, and reliable.

A clinician first makes an ADHD diagnosis and then uses the NEBA Report for confirmation or as support for further clinical testing.

NEBA is not a stand-alone diagnostic. The device is NOT to be used as a stand-alone in the evaluation or diagnosis of ADHD.

General NEBA Information (PDF)

Recent Events

Lexicor Medical Technology employee, Linda Stone earns Regulatory Affairs Certification (RAC)
January 6, 2011
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Qualifying Therapeutic Discovery grants cap year of successful NEBA® milestones.
November 5, 2010
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NEBA® receives Health Canada Medical Device License -- Key step for NEBA®
September 16, 2010
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NEBA® garners CE Mark -- EEG-based assessment aid specifically indicated for ADHD, key step for neuropsychiatric assessment aids.
July 07, 2010
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Lexicor Medical Technology Achieves ISO 13485 Certification March 29, 2010
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NEBA® is CE marked and Health Canada licensed. NEBA® is not approved for marketing in the U.S.A.
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