BEUDAMED
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    FRONTIER DEVICES NEURO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950017287·RETRACTOR ARMY/NAVY 2 PER SET D/E 8-1/2" 21CM

    Axcent Acrylics

    FDA UDI
    GARRECO, LLC·D79331002050·Premium Lt Fiber 5lb

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948004793·DURAVENT 2 IC, SIZE 5

    LISTER BANDAGE SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896046481·LISTER BANDAGE SCISSORS

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869634724·MOSS VRS Locking Cap Inserter, star 27, AO coup...

    EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BD PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 8, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·May 16, 2011

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Other ·STAAR SURGICAL COMPANY·Product code MTA·July 31, 2008

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 12°, STERILE, SINGLE USE

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·May 24, 2023

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    ILLUMISITE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·December 27, 2024

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 30°, STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 6, 2023

    HF-RESECTION ELECTRODE, LOOP

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 2, 2023

    NIM® 3.0 MAINFRAME INTERNATIONAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·May 6, 2023

    Right Heart Catheter Product Line: Catalog Number 604000------417D1006I.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code DYG·May 25, 2005

    Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Recall
    Open, Classified ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025