EEG / EMG in Colorado

D.O. Weaver and Company is a leading manufacturer of EEG and ECG electrode preparation and conductive products for cardiac diagnostics, sleep diagnostics, and electroneurodiagnostics applications. Based in Aurora, Colorado, the company specializes in high-performance skin prep gels and conductive pastes designed to reduce impedance and improve signal quality in diagnostic monitoring. Their flagship products—Nuprep Skin Prep Gel and Ten20 Conductive Paste—are trusted by technologists and technicians worldwide for reliable electrode adhesion and conductivity. ISO 13485 certified, Weaver and Company maintains rigorous manufacturing standards and distributes globally through an established distributor network.

Neurotron, Incorporated is a US-based medical device manufacturer established in 1981, headquartered in Aurora, Colorado. The company specializes in the Neurometer® CPT® (Current Perception Threshold), a proprietary neurodiagnostic device for painless, non-invasive sensory nerve fiber testing. The Neurometer® CPT® evaluates small unmyelinated C-fibers, small myelinated Aδ-fibers, and large myelinated Aβ-fibers at any cutaneous site, detecting >90% of sensory nerve fiber types using a standardized, double-blind automated test procedure. FDA-cleared since 1986, the device has been used in over one million tests globally and is supported by more than 800 peer-reviewed publications. The technology quantifies both hyperesthesia and hypoesthesia, monitors nerve regeneration progression, and enables early detection of nerve damage from diabetes, carpal tunnel syndrome, spinal injury, sciatica, radiculopathy, and polyneuropathy. Unlike traditional electrodiagnostic and biopsy procedures, CPT® measurements are unaffected by skin temperature, edema, or electromagnetic interference. The device is portable, battery-powered, painless, non-invasive, and requires no special environmental shielding. Neuval® CPT® software evaluates results against established norms, manages patient records, and generates clinical reports. The company markets through direct sales and an international distributor network across China, Japan, Switzerland, Korea, Benelux, UAE, and Kuwait. Products are manufactured in the USA.

WAVi Co manufactures the WAVi Scan, an FDA-cleared Class II EEG system designed for objective brain assessments in clinical, research, and performance contexts. The integrated platform combines a comfortable wet EEG headset (requiring no gel), cloud-connected software with guided protocols, and automated reporting. WAVi Scan includes evoked response testing (P300), Flanker tasks, and Trail Making Test assessments, with output metrics covering brain response voltage, latency, and quantitative EEG (QEEG) measures compared to reference ranges. The system is designed for non-specialist operation, with typical patient setup in 5–10 minutes and no requirement for specialized neurology staff. Primary applications include injury and performance monitoring (baseline/follow-up, return-to-activity programs, post-event documentation), longitudinal wellness tracking in primary care settings, and research initiatives. WAVi has been integrated into university research programs and institutional collaborations including NIH-affiliated studies and academic medical centers. The platform emphasizes structured workflow, training support via a user portal, and professional review functionality for qualified clinicians. Regulatory status: FDA 510(k) clearance as Class II medical device.