CeramTec receives FDA Breakthrough Device designation for novel ceramic knee project

The U.S. Food & Drug Administration (FDA) has confirmed that CeramTec’s novel ceramic total knee replacement device and proposed indication for use meet the criteria of a Breakthrough Device.

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Two-piece zirconia implant concepts are appropriate for clinical application

A review of the evaluation by ESCI of two-piece ceramic implant designs.

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Design inspired by Anatomy

The anatomically contoured BIOLOX CONTOURA® ceramic femoral head.

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