Clinical & Healthcare
Bring programmable bioelectric medicine into the workflows where chronic pain is actually managed.
Electrome is headquartered in Honolulu, Hawaii, on the island of Oʻahu. Hawaiʻi is an especially fitting home for our work: a cultural and geographic crossroads where Eastern healing traditions and Western medicine meet.
From Honolulu, we are building an AI-native platform for bioelectric medicine. Our commercial foundation begins with FDA-cleared devices for pain; our human-led Discovery R&D layer connects evidence, modeling, experiments, validation, and documentation.
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The therapeutic infrastructure layer for bioelectric medicine. FDA-cleared today, programmable for what comes next.
Every living system runs on a hidden electrical operating system that governs healing, inflammation, immunity, and regeneration. Electrome is decoding that language and turning it into precision therapies.
We begin with an FDA-cleared commercial foundation in pain, then apply AI-native Discovery R&D to organize evidence, challenge hypotheses, model signals, and support controlled scientific experiments. Scientists and appropriate regulatory pathways determine what can responsibly move forward.
Three integrated pillars connect discovery, controlled laboratory work, and future translation. Evidence and wet-lab data inform exploratory AI-assisted modeling; scientists review the results; validated programs follow the appropriate scientific and regulatory pathway.
AI-guided mapping of the electrome, decoding how signal profiles modulate ion channels, membrane potentials, and inflammatory pathways across cell types.
Programmable applicator concepts in development, building on the FDA-cleared ActiPatch foundation.
Research toward EHR-ready (FHIR) data workflows connecting devices, providers, and researchers.
MATRIX Platform Architecture
Electrome's AI-native Discovery R&D software pipeline and proposed MAT-based hardware vision. Hardware systems are conceptual and not cleared for medical, diagnostic, or therapeutic use.
Active AI-native R&D pipeline
Proposed hardware vision (concept and design)
Future Research ConceptNot an existing clinical system. Not cleared for diagnostic or therapeutic use. Does not process live patient data.
We start where the evidence is strongest, pain, inflammation, and wound healing, then expand into concussion, infection, dementia, and oncology.
Electrome's current foundation includes FDA-cleared devices developed and manufactured by BioElectronics Corporation. We welcome conversations with researchers, providers, retailers, pharmacies, rehabilitation clinics, health systems, and technology teams about future collaboration.
Explore the clinical, research, commercial, and technology collaboration areas Electrome supports.

Co-founder, Chief Executive Officer & Chief Technical Officer
Erik is a physicist and entrepreneur with advanced degrees in electrical engineering and mathematics who has spent 25+ years building bioelectric recording, control, and stimulation systems, securing multiple patents, contributing to multiple successful exits, and leading work across NIST ATP, NIH, and DARPA programs. As CEO, he sets the company's strategic direction and aligns its science, technology, and commercial roadmap around a single goal, making FDA-cleared bioelectric therapy broadly accessible. He brings the rare combination of deep technical fluency and the disciplined execution and capital formation needed to build Electrome into a leader in bioelectric medicine.

Co-founder & Chief Medical Officer
Dr. Nev Zubcevik is a board-certified physician and former Harvard Medical School faculty member and Medical Director at Spaulding Rehabilitation Hospital, with deep expertise in musculoskeletal medicine, traumatic brain injury, concussion, and non-pharmacologic pain management. She is also a prolific inventor and researcher whose work spans bioelectric signaling, regenerative medicine, and chronic Lyme disease, including the LymeCure research collaboration with Tulane University, alongside peer-reviewed research on non-opioid recovery. At Electrome she directs clinical strategy, evidence generation, and the integration of bioelectric therapy into mainstream care pathways.

Chief Commercialization Officer
Danny Rubenstein is a commercial operator and strategic advisor with 40+ years across consumer products, food, and emerging businesses. He has held CEO, COO, and CFO roles, was an original partner in Naked Juice and has served as member of operating leadership teams with several startup and early stage companies. Danny applies a regenerative, whole systems approach, advising founders and leadership teams on strategy, growth and developing organizational capacity. At Electrome he leads commercialization strategy, channel development, and revenue execution.

Scientific Advisor, Clinical Marketing & Sales Development
Shari O'Connor is a neuroimmunology expert with 30+ years advancing brain and immune-system therapies, with board-level credentials in Neurology, Immunology, Nutrition, and Pharmacogenomics. Her published research spans encephalopathy, brain trauma, and immune-mediated neurological disease, and she has advised programs translating neuroscience research into pharmacy practice and clinical care. At Electrome she leads clinical marketing and sales development, translating the evidence base into the form clinicians, channel partners, and payer audiences evaluate and buy on. In a category where adoption is won on clinical credibility rather than promotion, her scientific standing is itself the commercial asset.

Medical Director
Dr. Samir S. Awad is Chief of Surgery and Operative Care Line Executive at the Michael E. DeBakey VA Medical Center in Houston, and Professor of Surgery and Vice-Chair for Surgical Quality and Safety at Baylor College of Medicine. A bioengineering graduate of Penn with surgical critical-care training at Michigan, he leads investigator-initiated clinical research across pain, wound healing, edema, and bioelectric therapeutics. At Electrome he serves as Medical Director, guiding FDA strategy and clinical evidence generation across the platform.

Licensing Advisor
Wanni Davis is a biotech strategist with 15+ years spanning translational science, venture development, and commercialization. As former Director of Industry Partnerships at Harvard-affiliated hospitals, she built and negotiated the industry alliances that move academic science out of the lab and into commercial development. At Electrome she serves as Licensing Advisor, leading partnerships, business development, and alliance operations across life sciences and biopharma, including partner agreements and the licensing pathway around Electrome's patent-pending portfolio.
We are not actively hiring publicly. Join the talent network and we will reach out as roles open across engineering, clinical, and commercial.
Health systems, payers, providers, retailers, and life science partners. Build the next generation of bioelectric pain care alongside our team.
Explore PartnershipsJoin the institutions and operators building the programmable future of bioelectric care.