Operating Instructions

ManualsBrandsKneeMo ManualsElectronicsKnee Pain Device

Introduction

Congratulations on purchasing The KneeMo®

The KneeMo® is a device designed to dramatically reduce knee pain and increase mobility for those with

Osteoarthritis (OA), knee injuries, or who are from knee surgery.

Safety Precautions & Warnings

The KneeMo® is not is not a substitute for medical advice. Always seek the advice of your personal

health care professional with any questions you may have regarding a medical condition.

How The KneeMo® Works

The KneeMo® is not a standard knee brace, but rather a set of motion sensing straps that are placed

above and below the knee. The sensors stimulate the large and small muscle fibers using non-electrical

energy. The stimulation interrupts the pain pathway as the brain processes the stimulation instead of

the pain, permitting more movement in the knee.

Long-term use can improve knee muscle development, strength, and function. By addressing both pain

and muscle atrophy, The KneeMo® can do what other pain solutions cannot. In clinical studies, The

KneeMo® significantly improved knee pain in both the immediate and long term (4 weeks).

Using The KneeMo®

Get to Know your KneeMo®

Your new device consists of an UPPER and LOWER band. Each device has an on/off button, an LED light,

a reset button (see image below). Note the upper band has the KneeMo® logo on the front of the unit.

Two neoprene and Velcro straps and a buckle are included to attach the device to the shank and calf

USB to USB-c split charging cable to charge The KneeMo® always charge both devices at the same time

(INSERT PICTURES)

Wearing The KneeMo®

In order to assure a proper fit, there are several ways to attach your straps to The

KneeMo®

Thread one side of the neoprene straps through the plastic opening on the device so the side of

the strap so the silicone logo is facing the body (Picture). Hold the device in place on your leg

and pull the other side of the neoprene strap through the loop and secure snugly around the

leg.

(Placeholder) Threading it so you can use the tri-glide and make the unit smaller

(Placeholder) Threading it with the tri-glide and a second strap to make it larger.

Summary of content (5 pages)

PAGE 1
Introduction Congratulations on purchasing The KneeMo® The KneeMo® is a device designed to dramatically reduce knee pain and increase mobility for those with Osteoarthritis (OA), knee injuries, or who are from knee surgery. Safety Precautions & Warnings The KneeMo® is not is not a substitute for medical advice. Always seek the advice of your personal health care professional with any questions you may have regarding a medical condition.
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Placement of the Brace You will get the most benefit wearing The KneeMo® on the skin, however it can be worn over tights or light slacks. Putting on the device (add pictures here) Operating Instructions Turning on the Device Once the device is on your leg, make sure your leg is straight so the two units can “talk” to each other.
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Who may use the Limited Warranty? This Limited Warranty is extended only to the original consumer purchaser of The KneeMo® during the Warranty Period, and only to purchases of The KneeMo® from an authorized retailer. This Limited Warranty does not extend to any subsequent purchaser, transferee, or other owner of The KneeMo®, or any purchases made from a retailer other than an authorized retailer.
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To request inspection and service under this Limited Warranty, contact our Customer Service Department at 1-888-688-0896, during the Warranty Period to obtain a Warranty Return Authorization (“WRA”) number. Our Customer Service Department will require proof of purchase to provide you a WRA number. No return shipments will be accepted, and no warranty services will be provided, without a WRA number.
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FDA A review of the Code of Federal Regulations Subchapter Title 21 H-Medical Device, Part 80 Physical Medical Devices, Subpart F Physical Medicine Therapeutic Devices indicates that this device meets similar standards to Sec. 890.5975 Therapeutic Vibrator and is a Class 1 device. The device is exempt from the premarket notification procedures. As such there are no known risks to the subjects beyond those associated with using similar Class 1 devices such as therapeutic vibrators or a soft knee braces.