TriMas expands cleanroom capabilities at Denver facility

TriMas announced that its Intertech business, part of the TriMas Life Sciences division, has expanded its cleanroom capacity at its Denver, Colorado, facility. The additional production space addresses increased customer demand for highly engineered components used in medical technology applications, such as for use in testing, vascular delivery and extraction applications. Intertech recently expanded its ISO Class 8 cleanroom molding and assembly capacity by an additional 3,400 square feet, including dedicated space for molding presses and secondary operation equipment. The addition complements Intertech’s existing 9,000-plus square feet of ISO Class 8 cleanroom capacity. In addition, TriMas has invested in additional cleanroom capabilities at a second facility in the Denver area, under Intertech’s existing ISO 13485 Medical Devices Quality Management Systems certification. “Our increased investments in the Life Sciences end market continue to be an important long-term strategic enhancement for TriMas,” commented Thomas Amato, TriMas President and Chief Executive Officer. “By expanding our cleanroom production capabilities, we are addressing the growing demand needs of our customers, while remaining at the forefront of stringent regulatory standards. This investment not only underscores our dedication to operational excellence and superior quality, but also reaffirms our commitment to serving the evolving needs of the Life Sciences sector.”