Latest News

510(k) Clearance Received for Endoform® Plastics and Reconstructive Matrix20 Dec 2016

Aroa Biosurgery has been granted U.S. Food and Drug Administration (FDA) 510(k) clearance for the company’s Endoform® Plastics and Reconstructive Matrix, which allows the company to market and sell this device in the USA.

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Aroa Biosurgery successfully raises additional capital to fund growth14 Oct 2016

Aroa Biosurgery has successfully raised additional capital from new and existing investors from the USA, Australia and New Zealand.

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Launch of Ovitex Reinforced Bioscaffolds13 Jul 2016

Aroa Biosurgery’s partner, TelaBio, Inc. announced today, the commercial launch of the Ovitex™ Reinforced Bioscaffolds (“RBS”) portfolio of products for use in ventral hernia repair and abdominal wall reconstruction in the USA.

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