Seisa Group is a premier full-service medical device manufacturer. SEISA offers end-to-end product support from its multiple facilities in North America and Europe. SEISA has partnered with industry-leading medical device companies on projects ranging from concept to production and product evolution. SEISA’s partners have benefited from leveraging SEISA’s strengths, including the following:
- Vertically integrated operations to speed time to market and control costs
- Expertise in manufacturing FDA Class I, II, and III products
- Mastery in engineering and executing product transfers between facilities
- Expansive experience with a range of materials and designs
- Expansion of partners’ production capability and capacity at optimal cost
With more than three decades of experience working with some of the world’s largest medical device companies, SEISA today is anchored by a regulatory-focused culture (FDA-registered, ISO-certified) committed to delivering lean initiatives to drive savings and improvements.
Seisa Group’s more than 1,500 employees are eager to expand medical device companies’ global manufacturing and development footprints while ensuring consistent quality throughout SEISA’s range of facilities.
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51-200 employees
View all SEISA employees
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Medical Devices
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9005 Montana Avenue,El Paso,Texas,US
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1983
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Medical Device Manufacturing, Medical Manufacturing, Medical Device Assembly
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Waldo Diaz is the CEO of SEISA.
The decision makers in SEISA are Arturo Valtierra, Damian Quezada, Gabriel Vejar, etc. Click to Find SEISA decision makers emails.
SEISA specializes in the manufacturing of a wide range of medical devices, including but not limited to surgical instruments, diagnostic equipment, and implantable devices. Our expertise extends to both sterile and non-sterile products, ensuring compliance with stringent industry standards.
In addition to manufacturing, SEISA provides comprehensive product support services, including design and development, regulatory compliance assistance, quality assurance, and supply chain management. Our goal is to partner with clients throughout the entire product lifecycle, from concept to market launch.
Quality is a top priority at SEISA. We implement rigorous quality management systems that comply with ISO 13485 and other relevant standards. Our facilities are equipped with advanced quality control technologies, and our team conducts thorough inspections and testing at every stage of the manufacturing process to ensure the highest standards are met.
SEISA serves a diverse range of industries within the medical field, including but not limited to surgical, orthopedic, cardiovascular, and diagnostic sectors. Our extensive experience allows us to tailor our services to meet the unique needs of each industry, ensuring that we deliver effective and innovative solutions.
Yes, SEISA has a dedicated team of regulatory experts who can assist clients in navigating the complex landscape of medical device regulations. We provide support in preparing documentation for FDA submissions, CE marking, and other regulatory approvals, helping to ensure that products meet all necessary compliance requirements.
SEISA is committed to sustainability and environmentally responsible practices. We strive to minimize waste and energy consumption in our manufacturing processes and actively seek out eco-friendly materials. Our goal is to produce high-quality medical devices while reducing our environmental footprint and contributing to a healthier planet.
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