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Trice Medical Receives FDA 510(k) Clearance for mi-eye 2 -

Trice Medical received FDA 510(k) clearance to market mi-eye 2, a disposable needle with integrated camera to support diagnosis of joint injury. 

The next-generation iteration of mi-eye technology is designed for use in diagnostic and operative arthroscopic and endoscopic procedures to illuminate an interior cavity through a natural or surgical opening. mi-eye 2 also allows injection or aspiration under direct visualization.

Platform enhancements include improved resolution, field of view, depth of field and overall visualization.

Sources: Trice Medical; ORTHOWORLD Inc.

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