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. In addition to its certified ISO Class 8 cleanroom environments, Intertech's manufacturing facility, located in Denver, Colorado, is also MedAccred®?

accredited.