Viant is a globally recognized single-source contract manufacturer specializing in high-precision medical devices and complex components. We partner with multinational MedTech OEMs and medical technology innovators to optimize product lifecycles, eliminate supply chain risks, and speed up time-to-market.
Whether engaging specialized single-source capabilities or outsourcing full turnkey device manufacturing, Viant combines rigorous ISO 13485 quality systems, advanced engineering, and flexible global production footprints to deliver life-changing medical products.
From initial tooling and material selection to automated assembly and sterile packaging, explore our comprehensive technical capabilities.
Structured New Product Introduction (NPI) framework engineered to de-risk development, streamline design transfers, and accelerate commercial launch schedules while maintaining 100% regulatory compliance.
Deep material science capabilities covering implant-grade thermoplastics, UHMWPE, fluoropolymers, medical silicones, as well as specialty metals including Titanium, Stainless Steel alloys, and Nitinol.
Over 80 years of specialized metal tubing expertise. We manufacture high-tolerance hypotubes, Nitinol cardiac components, surgical reamers, and complex minimally invasive surgical instruments.
Advanced custom extrusion processing producing micro-lumens, multi-lumen tubing, co-extrusions, radiopaque lines, and jacketed braids for vascular catheters, drug delivery, and respiratory care.
State-of-the-art injection molding capabilities operating in certified cleanroom environments. Specializing in high-cavitation, multi-shot, insert molding, and overmolding for critical fluidics and surgical housings.
Specialized manufacturing facility producing sub-gram, micro-geometry medical components smaller than a single resin pellet, ideal for bioelectronics, microfluidics, and ophthalmic implants.
Internal mold building centers providing prototype and production-grade tooling. Using SolidWorks™ and Autodesk™ Moldflow simulation to minimize lead times and ensure long-life mold durability.
End-to-end device assembly services ranging from manual sub-assemblies to fully automated high-volume lines. Full sterile packaging validation, pouch/blister sealing, and sterilization coordination.
Viant maintains an unyielding commitment to patient safety, regulatory compliance, and operational excellence across all 26 manufacturing facilities.
FDA registered and ISO 13485 certified quality management systems supporting Class I, II, and III medical device production.
Comprehensive IQ/OQ/PQ validation protocols ensuring reliable, repeatable manufacturing process outputs.
End-to-end lot tracking, ERP control, raw material certification, and rigorous inspection metrics for regulatory submission support.
Global dual-sourcing options, regional nearshoring/onshoring networks, and vertical integration to insulate OEMs from disruptions.
Speak with our engineering specialists today to discuss technical specifications, material selection, prototyping timelines, or full contract manufacturing proposals.