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    Straumann Manufacturing, Inc.

    FDA registration
    Straumann Manufacturing, Inc.·4 products·🇺🇸 United States

    Straumann Manufacturing, Inc.

    FDA registration
    Straumann Manufacturing, Inc.·11 products·🇺🇸 United States

    STRAUMANN MEMBRANE FLEX

    FDA Adverse Event
    Injury ·COLLAGEN MATRIX, INC.·Product code NPL·May 28, 2025

    0001222315-2022-11593

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·May 30, 2022

    0001222315-2022-13297

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·June 20, 2022

    0001222315-2021-20514

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·November 22, 2021

    0001222315-2022-13803

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·June 30, 2022

    DENTAL IMPLANT NEODENT

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·July 23, 2024

    0001222315-2023-000788

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·January 12, 2023

    0001222315-2025-002824

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·October 9, 2025

    0001222315-2025-003371

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·November 27, 2025

    0001222315-2022-08557

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·April 29, 2022

    0001222315-2022-06865

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·April 8, 2022

    0001222315-2022-06867

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·April 8, 2022

    0001222315-2022-08036

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·April 22, 2022

    0001222315-2023-017444

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·July 17, 2023

    Implant, endosseous, root-form

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·December 29, 2025

    Implant, endosseous, root-form

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·December 29, 2025

    0001222315-2025-002709

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·September 29, 2025

    0001222315-2025-002709

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·September 29, 2025