BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MIM SOFTWARE INC.

    Reg #: 3004363352 · FEI: 3004363352 · Expires 2026
    View on FDA
    Products
    8
    Proprietary Names
    38
    Establishment Types
    2
    Classifications
    8

    Registration Details

    Registration Name
    MIM SOFTWARE INC.
    Registration Number
    3004363352
    FEI Number
    3004363352
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    25800 Science Park Dr Ste 180
    City
    Cleveland
    State
    OH
    ZIP
    44122
    Country
    US

    Regulatory Submissions

    510(k) Number
    K243012

    Owner / Operator

    Firm Name
    MIM Software Inc.
    Operator Number
    9057943
    Address
    25800 Science Park Drive, Suite 180
    City
    Cleveland
    State
    OH
    Postal Code
    44122
    Country
    US
    Correspondent
    Shekhar S Ganore

    Products

    Device Name Product Code
    Device, Digital Image Storage, Radiological LMB
    System, Image Processing, Radiological LLZ
    Radiological Image Processing Software For Radiation Therapy QKB
    System, Planning, Radiation Therapy Treatment MUJ
    Accelerator, Linear, Medical IYE
    Medical Device Data System OUG
    Radiological Image Processing Software For Ablation Therapy Planning And Evaluation QTZ
    Camera, Scintillation (Gamma) IYX

    Proprietary Names

    VueMe MIMcloud MIM- Symphony HDR Fusion Symphony HDR MIM-Symphony HDR Contour ProtegeAI Contour ProtegeAI+ MIM Encore MIM Maestro MIMpacs MIM 3D US Contour ProtegeAI (2 models) MIM MIM-Thin Client (mobile) MIM-LesionID Pro LesionID Pro Contour ProtegeAI (3 and 3.1 models) MIM-Dose Analysis Contour ProtegeAI (4 models) CPAI+ MIM Symphony DxLite MIM Symphony LDR MIM Symphony Dx MIM Symphony Bx MIMneuro MIM SurePlan MRT MIM SPECTRA Quant MIM SPECTRA Recon MIMcardiac MIMfusion MIM Harmony MIM-Ablation MIM - Centiloid Scaling MIM SurePlan LiverY90 MIM - Monte Carlo Dosimetry MIM on Linux Mobile MIM (2D and RT) MIM-Additional Tracers

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device