BEUDAMED
    FDA Registration Active 🇺🇸 United States

    50-S XL

    Reg #: 2936485 · FEI: 2936485 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    21
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    STRYKER ENDOSCOPY
    Registration Number
    2936485
    FEI Number
    2936485
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5900 Optical Ct
    City
    SAN JOSE
    State
    CA
    ZIP
    95138
    Country
    US

    Regulatory Submissions

    510(k) Number
    K071859

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Arthroscope HRX

    Proprietary Names

    50-S XL RF 2 PROBES, AARDVARK RF 2 PROBES, LATERAL RF 2 PROBES, HOOK 30 S GRIZZLY FINAL PACKAGING HOOK XL RF 2 PROBES, 90-S RF 2 PROBES, DIRECT RF 2 PROBE, MICRO-BRUSH RF 2 PROBES, 90-S MAX 90-S XL RF 2 PROBES, 50-S RF 2 PROBES, MICRO-CLAW SERFAS ENERGY SUPER 90-S CrossFire 2 90-S Accelerator Stryker Crossfire System CROSSFIRE UPGRADE USB DONGLE STRYKER CONSOLE CUSTOMIZER FR 2 PROBES, CONTOUR RF 2 PROBE, 90-DEGREE

    Establishment Types

    Manufacture Medical Device