Geistlich Surgery introduced Nexo-Gide® Dual Surface Membrane, which is FDA 510(k)-cleared for the management and protection of tendon injuries in which there has been no substantial loss of tendon tissue.
Nexo-Gide is a resorbable, highly purified, naturally dual surface bilayer (and therefore structurally optimal) collagen membrane for the management and protection of tendon injuries. The porcine-derived (Collagen I/III) membrane serves as a biocompatible protective encasement to support the body’s healing process. The product is manufactured using a patented process.
Geistlich Surgery introduced Nexo-Gide® Dual Surface Membrane, which is FDA 510(k)-cleared for the management and protection of tendon injuries in which there has been no substantial loss of tendon tissue.
Nexo-Gide is a resorbable, highly purified, naturally dual surface bilayer (and therefore structurally optimal) collagen membrane for the...
Geistlich Surgery introduced Nexo-Gide® Dual Surface Membrane, which is FDA 510(k)-cleared for the management and protection of tendon injuries in which there has been no substantial loss of tendon tissue.
Nexo-Gide is a resorbable, highly purified, naturally dual surface bilayer (and therefore structurally optimal) collagen membrane for the management and protection of tendon injuries. The porcine-derived (Collagen I/III) membrane serves as a biocompatible protective encasement to support the body’s healing process. The product is manufactured using a patented process.
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