Quality is critical to our business because lives depend on us.
The people behind Viant understand that we’re not just manufacturing products—we’re making components and finished devices that will be used to save or enhance a patient’s life. Our Global Quality Vision and Quality Policy are designed to ensure consistent high quality and compliance at every location, on every project, at every stage of the product lifecycle.
We mold, manufacture, and sterilize components and finished medical devices that are used to save or enhance patients’ lives every day. Consequently, we are committed to achieving the highest standards of quality along with regulatory compliance in everything we do. To achieve this vision, we pledge to maintain a medical device manufacturing culture with our mantra: THINK QUALTY. BE QUALITY. GO BEYOND.
MedPlast is committed to meeting customer, quality, regulatory, and safety requirements, as well as increasing customer satisfaction through continual improvement of services, processes, and technology.
Regulatory and Compliance
With 35+ 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
- FDA Registered and compliant with the Quality System Regulation
- ISO 14971 Risk Management Certified
- Class I, II, and III devices, including Premarket Approval (PMA) product support
- ISO 7 and ISO 8 Certified Cleanroom Controlled Environments
- Metrology laboratories
- Bioburden laboratory