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Steris proposes new sterilization system to FDA

Mentor manufacturing and technology company Steris Corp. has asked the Food and Drug Administration to approve a new chemical sterilization system for sale. The request is aimed at addressing the regulator’s concerns about changes to the company’s System 1 sterilizer.

MENTOR, Ohio — Mentor manufacturing and technology company Steris Corp. has asked the Food and Drug Administration to approve a new chemical sterilization system for sale.

Once approved, the yet unnamed system eventually will replace System 1, the first medical instrument sterilizer launched by Steris in 1988.

The premarket approval filing by Steris is aimed at putting to rest issues raised in a warning letter from the FDA in mid-May, Steris said in a written statement. The FDA said that Steris probably should have notified the federal regulator of substantial changes made to System 1 over the two decades it has been sold.

Steris will continue to service and support System 1 until at least 2011, said Steve Norton, corporate communications director for the company. “There’s no change in clinical practice required on the part of our customers,” Norton said.

“We’re in the process now of reaching out to all our U.S. customers to explain what we announced today,” he said.