BEUDAMED
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    Amvex Vacuum Regulator

    FDA UDI
    OHIO MEDICAL, LLC·00628101502041·VR-LL series, VacReg, Int 2Mode 200mmHg, Analog...

    LLN INSTRUMENTS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LXH·November 22, 2012

    SUMMIT MEDICAL

    FDA UDI
    Summit Medical, Inc.·00385640061261·

    N/A

    FDA UDI
    SHIPPERT MEDICAL TECHNOLOGIES, INC·00812185034448·

    BTK TURBOHAWK

    FDA Adverse Event
    Injury ·COVIDIEN, LLN·Product code MCW·November 5, 2015

    PERLA ® TL

    FDA UDI
    SpineArt SA·07640450867650·HOOK OFFSET LEFT LARGE

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·June 25, 2012

    CASE IV

    FDA Adverse Event
    Injury ·WR MEDICAL ELECTRONICS·Product code LLN·June 18, 1999

    CASE IV

    FDA Adverse Event
    Injury ·WR MEDICAL ELECTRONICS CO.·Product code LLN·April 29, 1997

    CASE IV

    FDA Adverse Event
    Injury ·WR MEDICAL ELECTRONICS·Product code LLN·December 10, 1999

    VIBRATION PLATE

    FDA Adverse Event
    Injury ·UNK·Product code LLN·April 9, 2026

    MOTOBAND CP IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·CROSSROADS EXTREMITY SYSTEM, LLC·Product code HWC·November 3, 2022

    MOTOBAND DYNAFORCE DYNABUNION

    FDA Adverse Event
    Malfunction ·CROSSROADS EXTREMITY SYSTEMS·Product code HRS·July 7, 2021

    SINGLE USE RETRIEVAL BASKET V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code LQR·August 29, 2025

    SINGLE USE RETRIEVAL BASKET V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code LQR·August 29, 2025

    SINGLE USE 3-LUMEN SPHINCTEROTOME V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·August 29, 2025

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·August 29, 2025

    SINGLE USE 3-LUMEN EXTRACTION BALLOON V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FGE·August 29, 2025

    SINGLE USE 3-LUMEN SPHINCTEROTOME V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·August 29, 2025

    MOTOBAND CP IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·CROSSROADS EXTREMITY SYSTEMS·Product code HRS·December 8, 2021