BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AR FABRICATING

    Reg #: 3010143171 · FEI: 3010143171 · Expires 2026
    View on FDA
    Products
    6
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    6

    Registration Details

    Registration Name
    AR FABRICATING
    Registration Number
    3010143171
    FEI Number
    3010143171
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    40132 Industrial Park Cir Ste 102
    City
    Georgetown
    State
    TX
    ZIP
    78626
    Country
    US

    Owner / Operator

    Firm Name
    AR Fabricating
    Operator Number
    10043437
    Address
    40132 Industrial park Cir., suite 102
    City
    Georgetown
    State
    TX
    Postal Code
    78626
    Country
    US
    Correspondent
    Thomas Siemer

    Products

    Device Name Product Code
    Appliance, Fixation, Spinal Interlaminal KWP
    Sacroiliac Joint Fixation OUR
    Thoracolumbosacral Pedicle Screw System NKB
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX
    Intervertebral Fusion Device With Bone Graft, Cervical ODP

    Proprietary Names

    Epiphany Channel Cervical Interbody Fusion System PLIF Peek Implant Lateral Peek Implant Cervical Peek Implant TLIF Peek Implant Cervical Interbody Fusion Lordotic Implant Cervical Interbody Fusion Neutral Implant Epiphany PSL Cage Epiphany PSE Cage

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)