BEUDAMED
    FDA Registration Active 🇺🇸 United States

    STALIF M FLX

    Reg #: 1225492 · FEI: 3001237338 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    NextPhase Medical Devices LLC
    Registration Number
    1225492
    FEI Number
    3001237338
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    88 Airport Dr
    City
    ROCHESTER
    State
    NH
    ZIP
    03867
    Country
    US

    Regulatory Submissions

    510(k) Number
    K173347

    Owner / Operator

    Firm Name
    NextPhase Medical Devices LLC
    Operator Number
    9026654
    Address
    88 AIRPORT DR.
    City
    Rochester
    State
    NH
    Postal Code
    03867
    Country
    US
    Correspondent
    James G Bennett

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    STALIF M FLX ACTILIF C FLX STALIF C FLX STALIF L FLX

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)