Certified Quality for Global Markets
ISO Certifications
Ultralife Corporation is a global provider of power solutions, communications systems, and electronic products for government & defense, commercial and industrial markets.
Overview
Ultralife is committed to delivering the highest standards of quality, environmental responsibility, and regulatory compliance across our operations. Our internationally recognized ISO certifications demonstrate our dedication to continuous improvement, customer satisfaction, sustainable business practices, and the development of safe, reliable products for the markets we serve. Explore our certifications below to learn more about the standards that support Ultralife’s commitment to excellence.
ISO 9001:2015
- Internationally recognized standard for quality management
- Registered Operations: New York (USA), Virginia (USA), Texas (USA), Massachusetts (USA), China, United Kingdom, Canada
ISO 9001 Quality System registration substantiates that Ultralife has policies, processes and procedures in place and that we are constantly striving to improve our product quality.
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- Ultralife Newark (HQ)
- Ultralife Comms Sys Division
- Ultralife Houston
- Ultralife Raynham
- Ultralife China
- Ultralife UK
ISO 14001:2015
- Internationally recognized standard for environmental management
- Registered Operations: China, United Kingdom
ISO 14001-registered Environmental Management System allows us to manage, monitor and control environmental issues and guides us to improve our environmental performance through more efficient use of resources and reduction of waste.
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ISO 13485:2016
- Internationally recognized standard for quality management – medical products
- Registered operations: New York (USA), Virginia (USA), Texas (USA), Massachusetts (USA), China, United Kingdom, Canada
ISO 13485 registration further indicates that Ultralife has a Quality System in place which drives us to provide safe and effective products in support of medical devices that consistently meet customer and regulatory requirements and facilitates market approval of products for medical device OEMs.
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