BEUDAMED
    32 results · 23ms · Sources: EU EUDAMED, US FDA

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    SIROLaser Blue

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    FINN KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304268890·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004893·35mm Gap Plate

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009511·PedFuse Reset, CNL, 5.0mm x 40mm

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034025·PedFuse Reset, CNL, 5.0mm x 25mm

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034018·PedFuse Reset, CNL, 5.0mm x 20mm

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034032·PedFuse Reset, CNL, 5.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009528·PedFuse Reset, CNL, 5.0mm x 45mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034005·35mm Gap Plate, Sterile, 5 Pack

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009535·PedFuse Reset, CNL, 5.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361009504·PedFuse Reset, CNL, 5.0mm x 35mm

    FIREBIRD SPINAL FIXATION SYSTEM, FIREBIRD SIDE-LOADING BODY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FORA P30 PLUS MULTI-MODE BLOOD PRESSURE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694065269·1.6 System 35mm Gap Plate Sterile Qty 2

    Distraction Paddle - 12mm

    FDA UDI
    CAPTIVA SPINE, INC.·00850065741673·Distraction Paddle - 12mm

    RD SET YI

    FDA Adverse Event
    Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

    RD SET DCI

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023

    MENICON ASRB (ASMOFILCON A) SILICONE HYDROGEL SOFT CONTACT LENS

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·March 18, 2026

    Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209

    FDA Enforcement
    Class II ·Terminated·Cadence Inc.·August 19, 2015

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·February 25, 2025