Through acquisitions and investments, we have been able to vertically integrated each step in the manufacturing process, from prototype to production technologies. This enables us to provide high quality services across the supply chain, strategically marrying high volume and high value capabilities. At Seisa, we offer completely customized solutions to manufacture your medical devices and components. We leave the choices to you, bringing our team of experts and engineers into any stage of the process to build the right combination of services to meet your needs. Backed by more than 35 years of medical device experience, Seisa prides itself in manufacturing high-quality devices that will positively impact lives.

Seisa is a medical device manufacturer serving every stage of the product life cycle including design and development, component manufacturing, and final assembly. Seisa delivers with full regulatory compliance.

With over 35 years of organic growth, Seisa Group provides a strong portfolio of resources and capabilities to meet your most challenging objectives.

At Seisa, commitment is central to every partnership. Our primary focus in every area of service is that what we manufacture, what we promise, and what we deliver could change a human life. From our founding, our core tenet has been to hold every employee responsible for adherence to FDA and international regulations.

That standard has been maintained from Seisa’s original plant established on the US-Mexico border in 1983, to the 350,000 square feet of manufacturing space we operate today across the globe. With 150,000 square feet of class 7 & 8 cleanroom capacity, 510K generation services, state-of-the-art prototyping and testing technology, and vertically-integrated device manufacturing capabilities, Seisa is fully equipped to provide a broad range of solutions to satisfy our customers’ requirements.

Our success is grounded in our communities. For nearly four decades, Seisa has emphasized the importance of investing in its people. Just as we value the people receiving our products, we value those who make them. In turn, our high retention and stable workforce underpins steady, mass-volume production.

Seisa at a Glance

Seisa was founded in 1983 by Julio Chiu, CEO and Chairman of the Board.

Our manufacturing sites are FDA registered and ISO 13485 compliant.

Our corporate headquarters is in El Paso, Texas.

Our presence spans four countries on three continents, with approximately 2,500 employees.

Seisa has successfully vertically integrated its offerings to customers through strategic acquisitions in molding, extrusion, and product design.

Seisa leverages its strategic global locations across North America, Europe, and Asia to offer full turnkey supply chain services to our customers.

We received the first of several FDA 510K approvals for Seisa devices in 2015.

We currently manufacture catheter-based products, implantable stents, tubing sets, pediatric and orthopedic-care products, among many others.

Seisa processes comply with FDA requirements for Class I, II, and III products.

Mold Making

Details