FDA-cleared copper oxide dressings are advanced wound care dressings designed to support healing in chronic and complex wounds. The dressings provide continuous antimicrobial protection and deliver bioactive copper ions that support angiogenesis, collagen formation, improved granulation, and regulated inflammation. This helps clinicians address stalled and hard to heal wounds with a safe, non-irritating, and clinically supported option.
Global Assurance LLC is a federal and state (VA) certified supplier that provides advanced medical and wound care products. We offer FDA-cleared copper oxide dressings that support chronic and complex wound management. Our bioactive copper technology promotes angiogenesis, collagen formation, improved granulation, cytokine regulation, and continuous antimicrobial protection. This gives clinicians a safe and effective option for stalled and hard to heal wounds.
Copper oxide dressings are soft, flexible, and moldable nonwoven dressings impregnated with copper oxide. They are moisture vapor permeable, non-irritating, and safe for prolonged use, with continuous copper ion activity and availability in both adhesive and non-adhesive formats. The bioactive copper technology supports angiogenesis, collagen formation, healthy granulation, and balanced cytokine activity while providing continuous antimicrobial protection. These combined properties help clinicians manage chronic, stalled, and complex wounds by maintaining a stable moisture environment and promoting effective tissue repair.
Copper oxide dressings are indicated for the management of wounds that benefit from a moist wound environment. This includes chronic and acute wounds such as diabetic ulcers, venous leg ulcers, pressure injuries, donor sites, surgical wounds, superficial burns, and partial thickness wounds. The dressings may be used on wounds with mild to moderate levels of exudate.
Do not use on patients with a known sensitivity or allergy to copper or any dressing components. Do not use on third-degree burns. Do not use on patients where occlusive dressings are contraindicated.
Use under the supervision of a healthcare professional. Monitor the wound regularly for signs of infection or deterioration. If redness, increased pain, excessive irritation, or abnormal wound conditions occur, discontinue use and evaluate the wound. Do not re-use the dressing. Single use dressing. Change frequency depends on wound condition and exudate level. The dressing may remain in place for up to 7 days as determined by clinical assessment. Remove the dressing prior to MRI procedures if required by facility protocols. For non-adhesive formats, a secondary dressing is required to secure the product. Avoid using the dressing in combination with topical agents that may interfere with copper ion activity unless directed by a clinician.
Localized irritation, sensitivity reactions, or discoloration of the surrounding skin may occur in rare cases. If adverse reactions appear, discontinue use and consult a healthcare professional.
Store in a cool, dry place away from direct sunlight. Keep the product in its original packaging until use. Do not use if the packaging is damaged or previously opened. Avoid excessive heat or moisture during storage.
Copper oxide
Nonwoven viscose rayon fibers and polypropylene layers that serve as the structural material for the dressing. These materials do not contribute antimicrobial or bioactive effects.
Acute Wounds
Burns
Cavity Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Infected Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Palliative Wounds
Pressure Ulcers
Sloughy Wounds
Superficial Wounds
Surgical Wounds
Venous Ulcers
Clean the wound according to standard clinical protocols and select an appropriately sized copper oxide dressing. Apply the dressing directly to the wound bed with the (orange) copper impregnated side facing the wound. Ensure full contact with the wound surface. For non-adhesive formats, secure the dressing with a clinically appropriate secondary cover. For adhesive formats, press lightly around the border to maintain proper placement. Use aseptic technique during application.
Gently lift the dressing from the wound bed using aseptic technique. If the dressing adheres lightly, moisten with sterile saline to ease removal. The dressing is single use and should be discarded after removal. Change frequency depends on wound condition, exudate level, and clinical judgment. The dressing may remain in place for up to 7 days when exudate levels are low, but more frequent changes may be needed for wounds with moderate drainage.
Non adhesive copper oxide dressings should be secured with a clinically appropriate secondary dressing such as a bordered foam, gauze wrap, conforming bandage, or adhesive retention sheet. Additional moisture management or protection layers may be used based on wound depth, exudate level, or anatomical location according to clinical practice guidelines.
The dressing consists of a nonwoven inner layer of viscose rayon fibers impregnated with copper oxide and an outer layer of polypropylene containing copper oxide particles. This multilayer design provides continuous copper ion activity, moisture vapor permeability, softness, and flexibility to support wound conformability and comfort.
Copper oxide dressings are supplied sterile for single use. They are warranted to be free from defects in materials and workmanship at the time of purchase when stored and used according to labeled instructions. No warranty is provided for reuse, reprocessing, or application outside of recommended guidelines.
CHG-compatible
Latex-friendly
Non-allergenic
Non-cytotoxic
Non-irritating
Product Type: Nonwoven wound dressing impregnated with copper oxide.
Active Ingredient: Copper oxide.
Inactive Components: Viscose rayon fibers and polypropylene layers used as the structural material of the dressing.
Construction: Multilayer design consisting of an inner nonwoven absorbent layer impregnated with copper oxide and an outer polypropylene layer containing copper oxide particles. The dressing is soft, flexible, moldable, and moisture vapor permeable.
Sterility: Sterile. Single use only. Individually packaged.
Copper Release Profile: Sustained release of low levels of copper ions during use to support antimicrobial activity and normal wound healing processes.
Conformability: High flexibility and moldability to match wound contours and irregular surfaces.
Moisture Vapor Transmission: Moisture vapor permeable to support balanced moisture management and help reduce maceration.
Adhesive Options: Available in adhesive and non adhesive formats.
Wear Time: May remain in place for up to 7 days depending on exudate level and clinician assessment.
Compatibility: Safe for use with standard therapeutic support surfaces such as low air loss, alternating pressure, powered redistribution, and air fluidized systems.
Latex Status: Contains no natural rubber latex.
Cytotoxicity and Biocompatibility: Non cytotoxic, non irritating, and hypoallergenic under normal use conditions.
Indicated Exudate Levels: Suitable for dry to moderate exudate levels.
Available Sizes:
2 x 2.4 inch Non-Adhesive
4 x 4.5 inch Non-Adhesive
4 x 8 inch Non-Adhesive
8 x 8 inch Non-Adhesive
2 x 2.2 inch Adhesive Format
2 x 8 Adhesive Format
4 x 4.5 inch Three Layer Dressing
1 x 7 inch Non-Adhesive
Dressings may be trimmed to fit wound dimensions using sterile technique.
Packaging: Individually sealed sterile pouches within labeled cartons.
Storage Requirements: Store in a cool, dry place away from direct sunlight. Keep in original packaging until application. Do not use if package is damaged.
Warranty: Guaranteed to be free from defects in materials and workmanship at the time of purchase when used and stored according to labeled instructions.
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