Kyphoplasty systems
Dfine
by Merit Medical Systems, Inc.
A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.
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Where to buy Dfine
Contact Merit Medical Systems, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From merit.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Procedures that use kyphoplasty systems
Frequently asked questions
What is Dfine used for?
A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.
Who makes Dfine?
Dfine is made by Merit Medical Systems, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Dfine come in?
The FDA device database does not list sizes for Dfine. Check the instructions for use or ask a Merit Medical Systems, Inc. representative.
Is Dfine MRI safe?
The FDA device database entry for Dfine does not state its MRI safety status. Check the labeling before MRI.
Is Dfine FDA cleared?
Dfine is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Merit Medical Systems, Inc. sales representative?
Merit Medical Systems, Inc. has not listed representatives on LA Vascular yet. Visit the Merit Medical Systems, Inc. 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.