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510(k) Data Aggregation

    K Number
    K162759
    Device Name
    KeraStat(R) Gel
    Manufacturer
    Date Cleared
    2017-06-02

    (245 days)

    Product Code
    Regulation Number
    N/A
    Why did this record match?
    Applicant Name (Manufacturer) :

    KeraNetics, LLC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    KeraStat® Gel is intended to provide a moist environment and absorb excess wound exudate. KeraStat® Gel is indicated for management of a number of partial thickness skin wounds such as: partial thickness (first and second degree) burns, severe sunburns, superficial injuries, cuts, and incisions/surgical wounds. Under the direction of a healthcare practitioner. KeraStat® Gel also may be used in the management of dry, light, and moderately exuding partial thickness wounds including: pressure (stage I-II) ulcers, venous stasis ulcers caused by mixed vascular etiologies, diabetic ulcers, donor sites, and grafts. KeraStat® Gel is not indicated for full thickness (third degree) burns. This device will be available by prescription.
    Device Description
    KeraStat® Gel is a sterile, non-implantable, water-based gelatinous (hydrogel) wound dressing intended to act as a protective covering in the management of a variety of partial thickness dermal wounds. KeraStat Gel is provided in a sterile, screw top tube for one-time use. Each tube contains 5 mL of KeraStat Gel, which contains 5% keratin protein rehydrated and polymerized in a water base, and is available by prescription from a healthcare professional.
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