BEUDAMED
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    ATLAS SPINE PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010036384·DOANE KNEE RETRACTOR LARGE BLADES ...

    JOBST SensiFoot

    FDA UDI
    BSN MEDICAL, INC.·00035664108427·SENSIFOOT 8-15 MM HG CREW MEDIUM BROWN 1 EN FR ES

    Prima Titanium Implant 4.2mmd/8mml

    FDA UDI
    DMI INNOVATIVE MEDICAL TECHNOLOGY LTD·07290112760012·"PRTI - is a self-tapping titanium dental impla...

    Posted Stainless Steel Archwire

    FDA UDI
    Ortho Arch Company Inc·D90911084213·.018 X .025 POSTED SS RIGHT FORM WIRES 42MM (10)

    PTA-PLUS PTA BALLOON CATHER 5 MM X 4CM, PTA-PLUS PTA BALLOON CATHETER 6MM X 4CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    STEM: AMISTEM H 01.18.133 HA COATED STD STEM SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 17, 2022

    CAIMAN DISP. INSTR. NON ARTICUL.D:5 / 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/ 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·February 27, 2015

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 9, 2013

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·September 23, 2014

    DYONICS GENERATOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY OKLAHOMA CITY MANUFACTURE·Product code GEI·June 2, 2011

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·November 15, 2023