Gosset Ownership
Private
Therapeutic Areas
Stage
Commercial
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Modalities
Ventris Medical General Information
Ventris Medical has received FDA 510(k) clearance for its Backpack® bone graft containment system and synthetic bone putty. The company’s products are designed to optimize cell proliferation and bone formation in orthopedic and spinal fusion surgeries. Their allograft fibers have demonstrated osteoinductive properties that promote stem cell differentiation into bone-forming cells. The company is recognized as an innovator in orthobiologics with a focus on both biologic and synthetic solutions.
Contact Information
Primary Industry
Surgical Medical Devices
Corporate Office
Newport Beach, California
United States
United States
Drug Pipeline
Amplify Bone Graft Putty
CommercialKey Partnerships
Ventris Medical Funding
No funding data available
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