Global OEM Engineering & Manufacturing Consultation

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Partner with Viant Medical to streamline your OEM medical device supply chain, reduce lead times, and leverage global cleanroom manufacturing expertise.

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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