BEUDAMED
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    LM-9300 ELMA Lithotripter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    VITROS

    FDA UDI
    ORTHO CLINICAL DIAGNOSTICS·10758750008476·VITROS Immunodiagnostic Products Vitamin B12/Fo...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613102562·Lempert Rongeur, Straight, 2.5mm Wide x 10mm Lo...

    ORTHODONTIC CERAMIC BRACKET

    FDA 510(k)
    FDA Class 2 ·Dental

    TWINHEADS TH-103 EXTRACORPOREAL SHOCK WAVE LITHOTRIPTER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 6, 2014

    PELVICOL ACELLULAR COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABS.·Product code FTL·April 12, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·June 20, 2011

    MITRACLIP G5 DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code NKM·November 13, 2025

    MITRACLIP G5 DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code NKM·November 21, 2025

    MITRACLIP G5 DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code NKM·September 19, 2025

    PKG, 3MM X 29CM INSERT, RIGHT ANGLE DISSECTOR, LONG JAW, P/N 0250282105 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

    FDA Enforcement
    Class II ·Terminated·Stryker Endoscopy·December 24, 2014

    TRICLIP G5 DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code NPS·November 26, 2025

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014

    PERI-STRIPS DRY WITH VERITAS COLLAGEN MATRIX (LINEAR CONFIGURATION)

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·July 29, 2014