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FDA Clears Exogenesis’ Hernia Mesh

October 3, 2019

Exogenesis received 510(k) clearance from the FDA for its hernia mesh, a device indicated for repairing abdominal wall hernias and abdominal wall deficiencies that require reinforcing material.

The device consists of monofilament medical grade polypropylene and has a surface treated with the company’s Accelerated Neutral Atom Beam technology.

The mesh provides long-term tissue support and its large pores encourage tissue ingrowth.

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