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TEI Biosciences Receives APMA Approval For PriMatrix

TEI Biosciences has reported that its PriMatrix Dermal Repair Scaffold has received the coveted American Podiatric Medical Association’s (APMA) Seal of Approval. PriMatrix is used in the management of diabetic and venous ulcers, second-degree burns, and surgical and trauma wounds.

APMA is the nation’s professional society for foot and ankle specialists. The Seal of Approval Program was created to inform podiatric physicians and consumers about products whose quality, safety and effectiveness promote good foot health.

In order to qualify for the Seal of Approval, PriMatrix had to pass a thorough scientific evaluation by a panel of APMA members. The results were then evaluated by a committee of Doctors of Podiatric Medicine (DPM) who decided to grant TEI the use of the Seal for PriMatrix.

PriMatrix dermal repair scaffold is an acellular collagen matrix derived from fetal bovine dermis, one of the purest forms of collagen available. Due to its bioactive collagen matrix technology, PriMatrix is an ideal material for the management of numerous types of wounds as it supports cell repopulation and revascularization processes essential to wound healing. PriMatrix is rich in Type III collagen, a natural component of fetal dermis that aids in tissue healing and regeneration.

PriMatrix is intended for the management of wounds that include: partial and full thickness wounds; pressure, diabetic, and venous ulcers; second-degree burns; surgical wounds; trauma wounds; tunneled/undermined wounds; and draining wounds.

Yiannis Monovoukas, chairman, president and CEO of TEI, said: “TEI is excited about APMA’s Seal of Approval award for PriMatrix. PriMatrix is a novel biologic product proven safe and effective in treating many types of skin wounds in several thousand patients. The addition of the APMA’s Seal of Approval to PriMatrix is an affirmation of our commitment to developing innovative healthcare products that better meet the needs of physicians and their patients.”