50+ Years at the Leading Edge of Medical Device Design & Manufacturing
Viant’s legacy of innovation stretches back to our first medical device manufacturing facility in 1968. Since then, we have strategically expanded our global footprint and engineering technical depth to offer vertically integrated, end-to-end solutions for global OEMs.
Our engineers bring deep industry-leading expertise across clinical and technical specialties. Operating within ISO 13485-certified and FDA-registered environments, we help MedTech partners accelerate speed to market, minimize supply chain risks, and deliver transformative medical devices worldwide.
50+ Years of Vertically Integrated Manufacturing Evolution
Over five decades, Viant has built a global infrastructure combining specialized technical centers of excellence with scalable nearshore and global manufacturing options.
Viant enters the medical device contract manufacturing market with precision metal tubing capabilities.
Expanded technical services into the orthopedic market, manufacturing critical implantable components.
Established our first medical-grade plastics injection molding facility to serve expanding MedTech needs.
Initiated full-service complex device assembly with a specialized focus on high-precision surgical tools.
Pioneered nearshore manufacturing facilities in Puerto Rico and Costa Rica for cost-effective global production.
Integrated UHMWPE orthoplastic components and established operational sites across North America, Europe, and Asia.
Rebranded as Viant; added advanced drug delivery combination device packaging and coating capabilities.
Expanded Bay Area D&D Hub and created the Complex Extrusion Center of Excellence alongside Costa Rica growth.
Acquired Knightsbridge Plastics to enhance micro-molding and in-house precision tooling suite for miniaturized devices.
Built for Engineers, Driven by Technical Innovation
Our leadership team comes directly from leading medical device OEMs. We intimately understand the regulatory pressures, stringent quality control standards, and rapid development timelines required in today’s healthcare market.
Viant bridges the gap between early-stage design feasibility and full-scale commercial manufacturing. Through 1:1 engineer-to-engineer collaboration, robust DFM (Design for Manufacturability), and validated process management, we ensure seamless transfer from concept to market.
Our Operational Values & Quality Culture
Every device we manufacture impacts patient outcomes. Our team operates with an uncompromising focus on quality assurance, continuous process improvement, and strict adherence to international standards.
Customer-Oriented
Partnering closely with global OEMs with a constant focus on patient safety, zero-defect quality, and mutual long-term success.
Uncompromising Integrity
Adhering to strict compliance, regulatory standardizations (ISO 13485, FDA 21 CFR Part 820), and ethical manufacturing practices.
Accountability & Ownership
Empowering engineering teams to make brave, data-driven decisions while remaining fully accountable for quality performance.
Operational Excellence
Driven by continuous OpEx culture across 25+ sites, reducing lead times, mitigating risk, and optimizing manufacturing costs.
Agile Manufacturing
Rapidly responding to design changes, supply chain shifts, and market opportunities through vertically integrated resources.
Unified Global Team
Collaborating seamlessly across continents under a shared mission: delivering high-quality, life-enhancing medical devices.
Partner with a World-Class Medical Device Manufacturer
Whether you require complex extrusions, nitinol metal tubing, micro-molding, or complete sterile device assembly, Viant offers the capacity, engineering skill, and global footprint to turn your concepts into market-ready realities.
Quality Systems & Certifications
- ✓ ISO 13485:2016 Certified Cleanroom Facilities
- ✓ FDA Registered & cGMP Compliant Operations
- ✓ ISO Class 7 & Class 8 Environmentally Controlled Cleanrooms
- ✓ Comprehensive Risk Management (ISO 14971)
- ✓ Full Lifecycle Verification, Validation & DFM Support