For healthcare professionals. The information on this page is intended for healthcare professionals. It is not a substitute for the manufacturer’s instructions for use, which accompany every device.
Company profile
About Joline
Joline is a family-owned German medical-technology manufacturer founded in 1999 in Hechingen. It designs and produces devices for dialysis, spine and cardiology. Its spine division concentrates on vertebral body augmentation, with kyphoplasty balloon catheters including a double-balloon concept, bone access instruments, cement filler devices and a closed cement mixing system.
Therapies
Clinical fields
Balloon kyphoplasty
Minimally invasive reconstruction of vertebral bodies after compression fractures using balloon catheters and bone cement.
Vertebral access & biopsy
Percutaneous instruments for reaching the vertebral body and sampling tissue.
Products
Product families
An overview of the main product families. Availability of individual products, references and sizes in Greece and Cyprus is confirmed on request.
Spine
Stop’n GO double-balloon catheter
A kyphoplasty catheter with two separately controllable balloons for vertebral body reconstruction.
Single-balloon catheters
Standard kyphoplasty balloon catheters with inflation and vacuum syringes.
Bone access instruments
Classic and one-step access instruments for percutaneous entry into the vertebral body.
Procedure kits
Ready-made sets combining access instruments, balloons and cement applicators, including single-pedicle versions.
Filler devices & QuattroMix
Cement applicators and a closed system for mixing and transferring bone cement.
Biopsy devices
Instruments for vertebral tissue sampling during augmentation procedures.
Product images: © Joline.
Novelties
What is new
EU MDR certificate
DEKRA (notified body 0124) issued EU MDR certificate 50565-60-03-02 for Joline’s vertebral augmentation devices, valid until 29 November 2030.
QuattroMix
A dedicated closed system for mixing and transferring bone cement in kyphoplasty.
CE marked · manufacturer certified under EU MDR 2017/745
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