BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LENSAR, Inc

    Reg #: 3009026057 · FEI: 3009026057 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    LENSAR, Inc
    Registration Number
    3009026057
    FEI Number
    3009026057
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    2800 Discovery Drive, Suite 100
    City
    Orlando
    State
    FL
    ZIP
    32826
    Country
    US

    Regulatory Submissions

    510(k) Number
    K173346

    Owner / Operator

    Firm Name
    LENSAR, Inc
    Operator Number
    10041040
    Address
    2800 Discovery Drive, Suite 100
    City
    Orlando
    State
    FL
    Postal Code
    32826
    Country
    US

    Products

    Device Name Product Code
    Ophthalmic Femtosecond Laser OOE
    Unit, Phacofragmentation HQC
    Laser, Ophthalmic HQF

    Proprietary Names

    LENSAR Laser System-fs 3D (LLS-fs 3D) Lensar Laser System-fs 3D (LLS-fs 3D) LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY LENSAR Laser System-fs 3D Lensar Laser System - fs 3D (LLS-fs 3D) ALLY Adaptive Cataract Treatment System LENSAR Laser System -fs 3D (LLS-fs 3D)

    Establishment Types

    Manufacture Medical Device