BioCer clears regulatory hurdles for hernia device

11/12/2013 |

BioCer has secured 510(k) clearance from the FDA for its TiO2mesh hernia-repair device, an implantable surgical mesh used during open and laparoscopic procedures to treat incisional or inguinal hernias. The mesh includes a hydrophilic coating that boosts handling and placement during surgery, reducing the requirement for added fixation.

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