BEUDAMED
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    SYNTHES VERTEBRAL SPACER TI

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526827905·ACHIMED ACHILLES SUPP BLACK II

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717101892·Burs FG 702, Pkg/100

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036019372·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450239568·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450166826·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450231449·

    BONYF AG

    FDA registration
    BONYF AG·5 products·🇱🇮 Liechtenstein

    TRACK 1.0 & 1.5 MM SYSTEMS-TISSUE REGENERATION BY ALVEOLAR CALLUS DISTRACTION

    FDA 510(k)
    FDA Class 2 ·Dental

    KIPPMED I.V. MANIFOLD

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD VENFLON¿ IV CANNULA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·August 17, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·November 29, 2022

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 25, 2007

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 25, 2013

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·March 7, 2011

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 23, 2021

    SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAK·March 21, 2023

    MARKSMAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code KRA·November 3, 2025

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medical-surgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. intended to be used by clinicians and medically qualified personnel for single or multiparameter vital signs monitoring of ambulatory and nonambulatory patients, including neonate, pediatric and adult patients. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medicalsurgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. The monitors can be used as stand-alone devices or as devices networked to an Acuity Central Station through wireless communication over a Welch Allyn FlexNet network.

    FDA Enforcement
    Class II ·Terminated·Welch Allyn Protocol, Inc·January 15, 2014