Westminster, Colorado | April 24, 2026
Cerapedics has announced a strategic supplier agreement with Vizient, significantly expanding access to its PearlMatrix® P-15 Peptide Enhanced Bone Graft, a Class III drug-device combination product designed for spinal fusion procedures in patients with degenerative disc disease (DDD). This agreement represents a major step toward broadening the availability of advanced bone regeneration technologies across hospitals, academic medical centers, and integrated healthcare networks in the United States.
PearlMatrix Drives Innovation in Bone Regeneration
At the core of this agreement is PearlMatrix®, the first and only bone growth accelerator clinically proven to enhance lumbar spinal fusion, powered by the proprietary P-15 Osteogenic Cell Binding Peptide. This peptide mimics a naturally occurring sequence in Type-1 collagen, enabling rapid attachment and activation of osteogenic cells, which are critical for new bone formation and tissue regeneration.
The product is FDA-approved for multiple lumbar interbody fusion procedures, including ALIF, TLIF, PLIF, OLIF, and LLIF, and is compatible with PEEK and titanium-based spinal implants. Clinical evidence from the ASPIRE TLIF Investigational Device Exemption (IDE) study demonstrated that PearlMatrix achieved more than double the fusion rates at six months compared to traditional autograft methods, highlighting its superior efficacy and accelerated healing potential.
Importantly, PearlMatrix has shown effectiveness even in high-risk patient populations, including individuals with obesity (BMI ≥30), nicotine use, and type 2 diabetes, making it a versatile and clinically valuable solution in complex surgical scenarios. These capabilities position PearlMatrix as a transformative advancement in orthopedic and spinal surgery, where achieving reliable bone fusion remains a key challenge.

