BEUDAMED
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    Volpara Imaging Software

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707014089·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 28

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127285·2.0 X 28mm Cannulated Headless Screw, T7

    LACTOSORB* SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036054045·

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIES (INSERTS)

    FDA 510(k)
    FDA Class 2 ·Dental

    NEOTRACT ANCHOR SYSTEM MODEL TAS400

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

    Herbert/Whipple®

    FDA UDI
    Zimmer, Inc.·00889024033931·

    BD ALARIS PRIMARY PUMP SET

    FDA Adverse Event
    Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·September 3, 2025

    LITHOVUE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGB·April 23, 2026

    IDENTITY XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 7, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

    ANN BLUNT TIP SCREW 4X52MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·May 30, 2024

    BLUNT TIP SCREW, ÿ 4X38MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·December 11, 2023

    ERBE'S CO2 TUBING/CAP SETS

    FDA Adverse Event
    Malfunction ·ERBE MEDICAL. LLC·Product code FEQ·April 7, 2026

    BLUNT TIP SCREW, ÿ 4X48MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·April 29, 2025

    CARINA

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·February 10, 2022

    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 9X58MM Item Number: 15-2028/14

    FDA Recall
    Open, Classified ·Linkbio Corp.·Product code HSX·March 21, 2023