• Easy to store, easy to use
• Versatile for use with a variety of wound types and sizes
• FDA cleared device (510(k))
• Biocompatible native human protein
• Resists protease degradation
• Stable at room temperature
• Requires no special storage, shipping, or preparation for use
• Long shelf life

ProgenaMatrix™ is indicated for dry and exuding partial- and full-thickness wounds such as: pressure (stage 1-4) and venous stasis ulcers, ulcers caused by mixed vascular etiologies, diabetic ulcers, donor sites and grafts, first- and second-degree burns, superficial injuries, cuts, abrasions and surgical wounds. ProgenaMatrix™ is not intended to be used on third-degree burns.

Federal (USA) law restricts this device to sale by or on the order of a licensed physician. Prior to use, read all package insert instructions and precautions. Do not use if the product package is damaged or opened. Do not use this device without the direction of an authorized health care professional. User should advise patient of appropriate precautions relevant to his or her case. Control any bleeding at wound site before applying matrix. Discontinue use if signs of maceration, odor or purulence are present, which may be indicative of infection. Must be used prior to expiration date. Do not re-sterilize. Discard any unused material. ProgenaMatrix™ is a fully hydrated matrix and does not absorb wound exudate; instead, it manages wound exudate through moisture vapor transmission and, if needed, fenestration.

Store between 2⁰C and 30⁰C.

Human keratin