For Podiatry, Foot & Ankle and Orthopedic Practices

The calf muscle pump, during the weeks it cannot work on its own.

Rx Only. FDA-cleared NMES device. Class II.

A prescription NMES device used at home by the patient, alongside casting, bracing and non-weight-bearing protocols.

Request Provider Info Pack Call (312) 804-1050
VEINOPLUS neuromuscular electrical stimulator with two self-adhering calf electrodes and lead wire
Who Prescribes

Podiatry, foot and ankle surgery, orthopedic trauma.

Setting

At home, operated by the patient on a prescribed schedule.

Practice Workload

No added in-office time and no equipment held by the practice.

What It Does

Used alongside the protocol you already set

VEINOPLUS® delivers neuromuscular electrical stimulation to the calf. It is prescribed by a physician, operated by the patient at home on a set schedule, and does not require in-office time or equipment managed by practice staff.

It is used alongside an existing protocol rather than in place of one. Casting, bracing and weight-bearing orders are unchanged.

Two self-adhering electrodes positioned over the calf, with the handheld stimulator held by the seated patient
Electrode placement over the calf. The patient operates the device seated.

How the patient uses it

1. Self-adhering electrodes are placed on each calf. No specialist application is required.

2. The patient selects the program. The device shuts off automatically at the end of a 60-minute session.

3. Used on the schedule the physician prescribes. It may be used while walking.

4. Pocket-sized, battery-powered and reusable — at home, at work or while travelling.

Practice Impact

What the practice has to do

Nothing is stocked, fitted or managed in the office. The device ships to the patient, the patient operates it, and the practice’s existing protocol is unaffected.

Inventory

None. No equipment is held by the practice.

In-office time

None added. No fitting or supervised session.

Existing orders

Casting, bracing, weight-bearing and rehabilitation plans are set by the practice and unchanged.

Prescribing Information

Indications & contraindications

Indications for use

Relaxation of muscle spasms; prevention or retardation of muscle disuse atrophy; increasing local blood circulation; muscle re-education; immediate post-surgical stimulation of calf muscles to prevent venous thrombosis; maintaining or increasing range of motion.

Contraindications

Cardiac pacemaker or other implanted electronic device. Active DVT at the treatment site. Severe arterial insufficiency. Uncontrolled congestive heart failure.

CautionFederal law restricts this device to sale by or on the order of a physician. Rx only.
Specifications

The device

Device class
Neuromuscular electrical stimulator, prescription only
Session length
60 minutes, with automatic shut-off
Power
Battery-powered, pocket-sized, reusable
Electrodes
Two self-adhering electrodes, one per calf, replaceable
Setting
Patient-operated, at home, on a prescribed schedule

Safety profile

Low-intensity impulses, with a waveform designed for patient comfort during stimulation. Reported skin reactions are rare, mild and self-limiting. The device is non-invasive, drug-free and patient-administered.

For The Practice

Questions practices ask

Does the practice have to stock anything?

No. Nothing is held, fitted or managed in the office.

Who operates the device?

The patient, at home, on the schedule the physician prescribes.

Does it change the immobilization protocol?

No. Casting, bracing and weight-bearing orders remain exactly as the practice sets them.

Can it be used alongside compression?

It may be combined with compression therapy at the physician’s direction.

Regulatory & Availability

Clearance and distribution

510(k)
K072252 — VEINOPLUS Neuromuscular Stimulator
Cleared
30 January 2008, Substantially Equivalent
Classification
21 CFR 890.5850 · product code IPF (powered muscle stimulator)
U.S. distributor
DynaPulse Medical LLC
Authorized distributor
C2 Medical Distributors LLC, Lake Mary, Florida
In use since
2004. 150,000+ patients across 40 countries (per DynaPulse Medical)
Federal availability
Available to VA and federal health systems on Federal Supply Schedule 36F79723D0020, held by Government Solutions and Services, LLC
Evidence

Published literature

Ten peer-reviewed publications and 49 international congress presentations are reported by DynaPulse Medical. Selected references are listed below for reference only; full texts are available on request.

Lobastov KV et al.
Int Angiol. 2014;33(1):42–49.
Griffin M et al.
Eur J Vasc Endovasc Surg. 2010;40:766–771.
Ryzhkin VV.
doi:10.17116/phlebo2017113131-141
Bogachev VY et al.
Int Angiol. 2011;30(6):567–590.
Zuccarelli F et al.
Angéiologie. 2005;57(2):48–54.
ELECTRO-PAD RCT
Le Faucheur A et al. Eur J Prev Cardiol. 2026. doi:10.1093/eurjpc/zwag080

Request the info pack

Instructions for use, indication details and ordering information. Clinicians and practice staff can request them directly.

Email C2 Medical
Telephone
(312) 804-1050
Email
[email protected]
HIPAA-secure fax
(321) 641-4230