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510(k) Data Aggregation

    K Number
    K113489
    Device Name
    ORION
    Date Cleared
    2012-07-27

    (247 days)

    Product Code
    Regulation Number
    878.4810
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Intra- and extra-oral surgery including incision, excision, hemostasis, coagulation and vaporization of soft tissue. The device is intended for use in the following procedures: Frenectomy, Frenotomy, Biopsy, Operculectomy, Implant Recovery, Gingivectomy, Gingivoplasty, Gingival Troughing, Crown Lengthening, Hemostasis of Donor Site, Removal of Granulation Tissue, Laser-assisted Flap Surgery, Debridement of Deseased Epithelial Lining, Incisions and Draining of Abscesses, Tissue Retraction for Impressions. Papillectomy, Vestibuloplasty, Excision of Lesions, Leukoplakia, Exposure of Unerupted / Partially Erupted Teeth, Removal of Hyperplastic Tissues, Treatment of Aphthous Ulcers, Sulcular Debridement, Pulpotomy, Pulpotomy as an Adjunct to Root Canal Therapy, and Light Activation of Bleaching Materials.

    Device Description

    The Orion laser system is a pulsed and cw diode laser emitting a wavelength of 980 nm, that is intended for ablating, excising and coagulation of intraoral soft tissue using a contact fiber optical delivery system.

    AI/ML Overview

    The provided 510(k) summary for the ASCLEPION LASER TECHNOLOGIES GmbH Orion laser system explicitly states:

    Nonclinical Performance Data: None
    Clinical Performance Data: None

    Therefore, no acceptance criteria, study details, or performance data are provided in this document. The device did not undergo performance testing to demonstrate its safety and effectiveness. Instead, its substantial equivalence to a predicate device (GENTLEray 980 K072262) was established based on having the "same principles of operation, with the same parameters and with the same indications for use."

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