Poseidon Nanosilver Hydrogel

Poseidon™ Nanosilver Hydrogel is an FDA-cleared advanced wound care product designed to support healing by maintaining an optimal moist wound environment while helping manage microbial burden. Its clear, non-sticky formulation combines moisture donation and absorption with nanosilver technology, making it easy to apply, monitor, and integrate into existing wound care protocols. Poseidon is intended for use across a range of wounds, including chronic, surgical, traumatic, and burn-related wounds.

Asclepii

Asclepii is a medical device company developing and commercializing next-generation wound care technologies. The company combines biomaterials, nanotechnology, and regenerative medicine to create products that improve healing, simplify clinical workflows, and expand access to advanced wound care. Its portfolio includes FDA-cleared products for wound management, with additional technologies in development for chronic wounds, surgical care, burns, and austere medical environments.

Website: https://asclepii.com
Benefits

• Helps maintain a moist wound environment that is conducive to healing
• Dual-action gel—absorbs and donates moisture (up to 13X its weight)
• Clear formulation permits wound visualization
• Conforms to irregular wound surfaces
• Proprietary Silver Nano structure allows for better surface area, being self-regulating and shelf-stable for antimicrobial control within the dressing
• Non-adherent, amorphous gel formulation
• Easy to apply and remove

Indications

Poseidon™ Nanosilver Hydrogel is indicated for the management of first- and second-degree burns and wounds including stasis ulcers, pressure ulcers, diabetic ulcers, lacerations, abrasions, skin tears, surgical incision sites, device insertion-site wounds, graft sites, and donor sites.

Contraindications

Do not use on patients with a known sensitivity or allergy to silver.

Storage Requirements

Store at controlled room temperature in a clean, dry location. Protect from excessive heat, freezing, and direct sunlight. Keep the container closed when not in use.

Inactive Ingredients

Deionized water, silver as nanoparticles, carbopol, sodium hydroxide

How Supplied/Sizing
1 oz (approximately 30 g), 3 oz (approximately 85 g)
HCPCS Code
Product features
cancel Antimicrobial format available
check_circle Clear
check_circle Compatible w/ topicals
check_circle Conforms readily to wound
cancel Limited shelf life
cancel Moisture vapor permeable
cancel Powder form
cancel Preserved multiple dose
cancel Secondary dressing required
cancel Unpreserved unit dose
cancel Usable on infected wounds
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
cancel Published Clinical Article Available
Recommended Use

Acute Wounds
Burns
Cavity Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Hypertrophic Scars/Keloids
Infected Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Palliative Wounds
Pressure Ulcers
Sloughy Wounds
Superficial Wounds
Surgical Wounds
Venous Ulcers
Lacerations; abrasions; skin tears; device insertion-site wounds; graft sites; donor sites

Mode of Use/Application

Use exactly as directed by the prescribing physician. Wash hands with soap and water before touching the wound. Carefully clean the wound using soap and water. Dispense sufficient gel onto a clean applicator, such as a tongue depressor or gauze, and liberally cover the wound. If desired, cover with gauze wrap, film, or a non-woven adhesive secondary dressing. Remove the product from the skin within 24 hours by cleaning the wound site with soap and water. Replace the cap and discard the remaining product.

Construction

Amorphous, water-based hydrogel containing silver nanoparticles, Carbopol, and sodium hydroxide.

Clinically Tested

CHG-compatible
Latex-friendly
Non-allergenic
Non-comedogenic
Non-cytotoxic
Non-irritating

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