BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    KREYENBERG GMBH

    Reg #: 3009455196 · FEI: 3009455196 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    KREYENBERG GMBH
    Registration Number
    3009455196
    FEI Number
    3009455196
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    Oststrasse 51
    City
    Norderstedt Schleswig-Holstein
    Country
    DE

    Owner / Operator

    Firm Name
    Kreyenberg GmbH
    Operator Number
    10044509
    Address
    Oststrasse 51
    City
    Norderstedt
    State
    Schleswig-Holstein
    Postal Code
    D-22844
    Country
    DE

    US Agent

    Business Name
    Emergo Global Consulting LLC
    Contact Name
    Yong Sun
    Address
    2500 Bee Cave Rd., Bldg. 1, Ste. 300
    City
    Austin
    State
    TX
    ZIP
    78746
    Country
    US
    Email
    [email protected]
    Phone
    512 3279997

    Products

    Device Name Product Code
    Rod, Fixation, Intramedullary And Accessories HSB
    Orthopedic Manual Surgical Instrument LXH
    Guide, Surgical, Instrument FZX
    Reamer HTO

    Proprietary Names

    T2 Flexible Nail SPEEDLOCK SLEEVE 200 SPEEDLOCK SLEEVE 180 SPEEDLOCK SLEEVE 170 Artemis - Lag screw guide sleeve Artemis - Repositioning guide sleeve Artemis - Channel tube 78010019 AGILON® reamer tapered

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)