Viant Medical
Directory listingDirectory record status
These labels describe this UNITEMFG record. They do not guarantee current capabilities, certifications, capacity, quality, or fit for a specific job.
- Directory listing
- Listed
- Ownership
- Unclaimed
- Last profile update
- Aug 13, 2026
About
Medical device design and manufacturing partner focused 100% on medical technology, providing end-to-end services from design to full-scale production with 80,000 sq. ft. facility.
Specialties
Manufacturing Capabilities
Processes
Certifications & Quality
Business Certifications
Source-backed capabilities
These capability statements were observed in the linked manufacturer sources. They are source evidence, not a certification of the company or its current capacity.
Certification
- FDA Registered
ed to exact specification, in full compliance with FDA guidelines. ISO 13485 Certified, Medical Device Single Audit Program (MDSAP) certified, and Class I, II, III, and combination devices, including Premarket Approval (PMA) Product Support Metrology and Microbiology Laboratories FDA registered and compliant with the Quality System Regulation cGMP ISO 7 and ISO 8 Certified Cleanroom Controlled Environments Quality & Supplier Resources Here you’ll find site-specific information, forms, and more.
Viant Medical certification evidence ↗ Observed Aug 14, 2026 - ISO 13485
asured quality objectives. Regulatory and Compliance With over fifty years of medical device experience, we have developed a thorough understanding of the complex regulatory environment. Every product is manufactured to exact specification, in full compliance with FDA guidelines. ISO 13485 Certified, Medical Device Single Audit Program (MDSAP) certified, and Class I, II, III, and combination devices, including Premarket Approval (PMA) Product Support Metrology and Microbiology Laboratories FDA r
Viant Medical certification evidence ↗ Observed Aug 14, 2026