BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider

    Reg #: 1056128 · FEI: 1000132435 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Stryker Sustainability Solutions Lakeland
    Registration Number
    1056128
    FEI Number
    1000132435
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5307 Great Oak Drive
    City
    LAKELAND
    State
    FL
    ZIP
    33815
    Country
    US

    Regulatory Submissions

    510(k) Number
    K220411

    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
    Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed NUJ

    Proprietary Names

    Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider

    Establishment Types

    Reprocess Single-Use Device