BEUDAMED
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    Centralite Patient Positioning Laser

    FDA UDI
    Diacor, Inc.·B237DLG40·Green Diode Sagittal Laser

    Centralite Patient Positioning Laser

    FDA UDI
    Diacor, Inc.·B237DLG20·Green Diode Cross Laser

    Centralite Patient Positioning Laser

    FDA UDI
    Diacor, Inc.·B237DLG60·Green Diode Sagittal Laser for Bodytom

    Huestis Centralite Patient Positioning Laser

    FDA UDI
    HUESTIS MACHINE CORPORATION·00850077007262·KIT CONTAINS 2 DLG-2 GREEN CROSS LASERS, 1 DLG-...

    ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND

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

    BARD

    FDA Adverse Event
    Other ·BARD ACCESS SYSTEMS INC.·Product code DQO·August 12, 1998

    PERC-DLG CONVENIENCE PACK

    FDA Adverse Event
    Other ·ARTHROCARE CORPORATION·Product code GEI·February 10, 2006

    PROTEGE IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·October 28, 2019

    AU600 CLINICAL CHEMISTRY ANALYZER WITH ISE

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·February 11, 2014

    TRILOGY MX

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC·Product code IYE·July 21, 2011

    VERSA HD

    FDA Adverse Event
    Malfunction ·ELEKTA LTD·Product code IYE·April 23, 2021

    UNKN COBLATION SPORTSMED DEV

    FDA Adverse Event
    Injury ·ARTHROCARE CORP.·Product code GEI·April 4, 2022

    SENSOR MMT-7040C1 GUARDIAN4 5PK OUS 1

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZP·January 29, 2025

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 19, 2020

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code QCD·December 12, 2024

    Coating, Liquid, Glc

    FDA classification
    FDA Class 1 ·Coating, Liquid, Glc

    AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, interochanteric fractures, high subtrochanteric fractures and combinations of these fractures, including non-union, malunion and tumor resections. The Long Nail system is additionally indicated to treat pertrochanteric fractures associated with shaft fractures, pathologic fractures in osteoporotic bone (including prophylactic use) of the trochanteric and diaphyseal areas, impending pathological fractures, long subtrochanteric fractures, ipsilateral femoral fractures, proximal or distal non-unions, malunions, revision procedures and tumor resections.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·June 7, 2017

    ALG WW LLC

    FDA registration
    ALG WW LLC·2 products·🇺🇸 United States

    ALLEVA MEDICAL (D.G.) LTD

    FDA registration
    ALLEVA MEDICAL (D.G.) LTD·13 products·🇨🇳 China

    DLP Medical Products, Corp.

    FDA registration
    DLP Medical Products, Corp.·1 product·🇺🇸 United States