SI-BONE, INC.

SI-BONE, INC. specializes in the design, development, and supply of advanced surgical implant systems for orthopedic and spinal applications, with a focus on proprietary bone fusion and prosthetic technologies. Their core capabilities center on the manufacturing of implantable medical devices, including spinal fixation systems, prosthetic limb components, and surgical bone hardware engineered for biocompatibility and long-term structural integrity. The company demonstrates deep technical expertise in minimally invasive implant design, load-bearing biomaterials, and precision manufacturing processes compliant with FDA and ISO 13485 standards. Their specialization in trauma and spinal reconstruction hardware—evidenced by products such as the iFUSE TORQ Implant System—positions them as a niche provider of high-performance, clinically validated solutions for complex musculoskeletal interventions. The company maintains a consistent relationship with the Department of Veterans Affairs, supplying critical orthopedic and prosthetic implants to support veteran rehabilitation and mobility restoration programs. Their work with the Department of Defense further underscores their role in equipping military medical systems with advanced surgical hardware for combat-related trauma care. These partnerships reflect a trusted, mission-aligned supply chain focused on durable, field-proven medical devices. SI-BONE operates primarily within NAICS 339113, which encompasses the manufacturing of surgical appliances and supplies, specifically implantable medical devices used in orthopedic, spinal, and limb reconstruction. Their market positioning is defined by innovation in spinal fusion technology and limb salvage systems, serving a specialized segment of the medical device industry focused on trauma, degenerative conditions, and post-surgical recovery. As a 2L entity headquartered in Santa Clara, California, SI-BONE, INC. is a mid-sized manufacturer with a focused operational footprint. While no federal certifications are listed, their consistent delivery of Class II medical devices to federal healthcare providers confirms adherence to rigorous regulatory and quality control frameworks required for government procurement.