Operio has been cleared for the US market

Toul Meditech AB is proud to announce that Operio has been cleared by the FDA according to 510(k) and that the device now can be marketed in the US.

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Operio is a portable device for use in a surgical operating room that produces a directed, non-turbulent flow of air to the surgical site during ophthalmic surgery and to the sterile instruments used during surgery.

Tomas Hansson, CEO Toul Meditech AB, 2016-07-25

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