Connect with Our Medical Device Engineering Experts
Whether you have a complex engineering challenge, require design for manufacturability (DFM) review, or seek full-scale contract manufacturing for high-precision medical devices, Viant Medical is equipped to support your technical requirements.
With 26 ISO 13485-certified global locations and over 300,000 square feet of ISO Class 7 and Class 8 cleanroom footprint, our technical teams provide seamless integration from prototyping to volume manufacturing.
Technical Consultation & Program Support
- Design for Manufacturability (DFM)
- ISO Class 7/8 Cleanroom Molding
- Precision Metal & Nitinol Tubing
- Sterile & Non-Sterility Device Assembly
- Process Validation & Quality Management
- ViaLaunch™ Program Management
Global Contact Information
Global Corporate Headquarters
2 Hampshire Street
Foxborough, Massachusetts 02035
United States of America
Telephone & Direct Support
North America: +1-508-543-2000
International Desk: +1-508-543-2000 (Ext. 4)
Business Hours: Mon-Fri, 8:00 AM - 5:00 PM EST
Commercial & Technical Inquiries
Email: [email protected]
Quality & Regulatory: [email protected]
Supply Chain Support: [email protected]
Global Manufacturing & Regulatory Compliance
Viant operates a fully integrated global network designed to provide regional risk mitigation, flexible onshoring options, and rigid quality assurance according to international medical standards.
26 Global Facilities
2.3 million square feet of advanced manufacturing space positioned strategically across North America, Europe, and Asia for optimal global supply chain resilience.
300K+ Sq. Ft. Cleanrooms
State-of-the-art ISO Class 7 and Class 8 environmentally controlled cleanrooms ensuring maximum purity for critical surgical, orthopedic, and diagnostic components.
ISO 13485 & FDA Registered
100% dedicated to medical technology. Comprehensive quality systems maintaining rigorous compliance with FDA, EU MDR, and global regulatory standards.
Request Product Catalog & Technical Specifications
Explore detailed technical datasheets, material compliance certificates, and capability profiles tailored for medical device original equipment manufacturers (OEMs).
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