After more than a year of review, the Food and Drug Administration has cleared for market the next-generation liquid chemical sterilizing system–System 1E–of STERIS Corp. The Mentor, Ohio, maker of ...

MENTOR, Ohio--(BUSINESS WIRE)-- STERIS Corporation (NYSE: STE) today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the STERIS SYSTEM 1E ® Liquid Chemical ...

STERIS Corp. (NYSE: STE) has settled with the Food and Drug Administration, addressing the “violating device” status of the company’s System 1 liquid chemical sterilizer and fleshing out a transition ...

Steris Corp. chief executive Walt Rosebrough on Tuesday announced the company's plans to build an $11 million facility in Mentor and add 300 jobs there over the next three years. The positions include ...

STERIS Corp. has received FDA’s 510(k) clearance for software modifications to its System 1E liquid chemical sterilant processing system, according to a FDA report and a MEDCity report.

Healthcare facilities now have 18 months to fully transition to an alternative reprocessing device from the Steris System 1 processor, according to news release from the U.S. Food and Drug ...

The Food and Drug Administration has warned doctors and hospital administrators that a widely used surgical tool sterilizer made by Mentor-based Steris no longer has the agency's "safe and effective" ...