Kyphoplasty systems

MEDINAUT-X(IBE System)

by Imedicom Co., Ltd.

A catheter-like device with an inflatable balloon at the distal end used for the reduction of fractures and/or creation of a void in cancellous bone [e.g., in the spine for a vertebral compression fracture (VCF), hand, tibia, radius, and calcaneus]. It is commonly used for kyphoplasty, which involves its insertion into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated. After the device is removed, orthopaedic bone cement is introduced into the created void to stabilize the vertebra. This is a single-use device.

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MEDINAUT-X(IBE System) models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
IBE-10β€” Not statedAvailable
IBE-15β€” Not statedAvailable
IBE-20β€” Not statedAvailable
IBE-B00β€” Not statedAvailable
IBEX10β€” Not statedAvailable
IBEX15β€” Not statedAvailable
IBEX20β€” Not statedAvailable

FDA clearances

  • 510(k) K153296 July 2016

Procedures that use kyphoplasty systems

Frequently asked questions

What is MEDINAUT-X(IBE System) used for?

A catheter-like device with an inflatable balloon at the distal end used for the reduction of fractures and/or creation of a void in cancellous bone [e.g., in the spine for a vertebral compression fracture (VCF), hand, tibia, radius, and calcaneus]. It is commonly used for kyphoplasty, which involves its insertion into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated. After the device is removed, orthopaedic bone cement is introduced into the created void to stabilize the vertebra. This is a single-use device.

Who makes MEDINAUT-X(IBE System)?

MEDINAUT-X(IBE System) is made by Imedicom Co., Ltd.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does MEDINAUT-X(IBE System) come in?

The FDA device database does not list sizes for MEDINAUT-X(IBE System). Check the instructions for use or ask a Imedicom Co., Ltd. representative.

Is MEDINAUT-X(IBE System) MRI safe?

The FDA device database entry for MEDINAUT-X(IBE System) does not state its MRI safety status. Check the labeling before MRI.

Is MEDINAUT-X(IBE System) FDA cleared?

MEDINAUT-X(IBE System) is covered by FDA submission K153296.

How do I contact a Imedicom Co., Ltd. sales representative?

Imedicom Co., Ltd. has not listed representatives on LA Vascular yet. Visit the Imedicom Co., Ltd. company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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