Kyphoplasty systems
Prolix
by Camber Spine Technologies, LLC
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
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Where to buy Prolix
Contact Camber Spine Technologies, LLC directly; they can quote, ship, or point you to the distributor for your country.
From cambermedtech.com, checked November 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Prolix models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| CW-107-001 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Prolix used for?
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
Who makes Prolix?
Prolix is made by Camber Spine Technologies, LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Prolix come in?
The FDA device database does not list sizes for Prolix. Check the instructions for use or ask a Camber Spine Technologies, LLC representative.
Is Prolix MRI safe?
The FDA device database entry for Prolix does not state its MRI safety status. Check the labeling before MRI.
Is Prolix FDA cleared?
Prolix is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Camber Spine Technologies, LLC sales representative?
Camber Spine Technologies, LLC has not listed representatives on LA Vascular yet. Visit the Camber Spine Technologies, LLC 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.