Trusted by 65+ Medical Device and Life Science Customers Worldwide
With more than 30 years of experience in product, sub-assembly, and PCBA manufacturing, Creation Technologies supports a global footprint of 13 strategically located facilities across the U.S., Canada, Mexico, and Asia. Our ISO 13485 certified operations are built for exceptional quality, speed, and regulatory compliance—ensuring your products consistently meet the highest standards.
Collaborate with Proven Medical Expertise
- ISO 13485:2016-certified
- FDA-registered sites
- Class I, II, III
- Pre-Market Approvals
- 21 CFR Part 11-validated business systems & electronic records
- Device History Records (DHR)
Protect & Sharpen Your Competitive Edge
- Extensive supply base partners
- Rigorous materials handling processes
- VISION Manufacturing Execution Systems (MES)
- Product Traceability to component level
- Counterfeit prevention
- Asset tracking & serialization
Accelerate Speed to Medical Markets
- Fast-track design and functionality validation
- Deep-domain Medical expertise
- Expert program management, quality
and regulatory approvals - Proven methodologies for product transfer and New Product Introduction (NPI)
Strategically Located Manufacturing Sites to Meet Your Critical Requirements
Find the location that best suits your needs—13 Locations, 4 countries (U.S., Canada, Mexico, China) and 3,000+ dedicated professionals.Â
Responsive Solutions for Your Entire Product Lifecycle
Contact us for the best total solutions.​
With expert manufacturing capabilities, state-of-the-art equipment and industry-leading best practices, Creation delivers maximum efficiency and optimum product quality end-to-end.Â
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