VEINOPLUS® reactivates the calf muscle pump to increase local blood circulation — using Second Heart Technology™, a proprietary low-frequency waveform that produces rhythmic calf contractions without painful muscle fatigue.
VEINOPLUS® is an FDA-cleared Class II neuromuscular stimulator. Coverage may be available through Medicare, commercial plans (e.g., Blue Cross Blue Shield), and the VA & federal health systems — eligibility, medical necessity, and reimbursement are determined solely by each payer and plan. Available to the VA and federal health systems on the Federal Supply Schedule (FSS 36F79723D0020).
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A pocket-sized, FDA-cleared NMES device built around a proprietary low-frequency waveform. Each rhythmic calf contraction increases local blood circulation — without painful muscle fatigue.
Engineered by its inventor, Dr. Jozef Cywinski, VEINOPLUS® uses a proprietary low-frequency waveform that sets it apart from general EMS or TENS devices:
VEINOPLUS® is a pocket-sized, lightweight, battery-powered EMS device. Using Second Heart Technology™, it delivers low-frequency, low-voltage impulses through two electrodes on the calf, producing rhythmic contractions that activate the calf muscle pump — the body's "second heart." Its proprietary signal waveform is designed for patient comfort during stimulation.
VEINOPLUS® technology has been studied in 10 peer-reviewed publications and presented at 49 international congresses, in collaboration with globally recognized vascular research teams. Published data demonstrate increased arterial inflow and venous return in the lower limbs during stimulation.
Use for at least 100 min/day (5 sessions × 20 min) significantly reduced post-surgical DVT incidence in high-risk patients vs. standard care alone.
In duplex-ultrasound studies, VEINOPLUS® increased peak venous velocity up to 11× and total venous volume flow up to 12× (20 → 240 ml/min) vs. passive baseline.
Rhythmic, stimulated calf contractions activate the muscle pump — increasing local blood circulation and maintaining muscle activity even when voluntary exercise isn't possible.
An FDA-cleared, pocket-sized electro-muscular stimulation (EMS) device available to the VA and federal health systems on Federal Supply Schedule. Used by 150,000+ patients across 40 countries, supported by clinical studies since 2004.


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