www.fdanews.com/articles/192955-fda-clears-exogenesis-hernia-mesh
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.