BEUDAMED
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    Smith and Nephew Suture Anchors - 5.0mm Absorbable Polymer Anchor, Smith and Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317, 7209318, Smith and Nephew Suture Anchors - Bioraptor 2.3 PK Suture Anchor, Smith and Nephew Suture Anchors - Osteoraptor Suture Anchor, Smith and Nephew Suture Anchors - Twinfix Ultra HA Suture Anchor, Smith and Nephew Suture Anchors - OSTEORAPTOR Curved Suture Anchors, Smith and Nephew Suture Anchors - Ultra Fast-Fix Meniscal Repair System, Ultra Fa

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POUR-PLUS

    FDA UDI
    Denplus Inc·D8451151105·POUR-PLUS, LPI, 454 g

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192473·Apex Revision Knee Reamer – ZIMMER LONG FLUTES,...

    Precontoured Rod Ø5.5 mm x105 mm Package

    FDA UDI
    XENCO MEDICAL LLC·B064XM21511051·SETX Ø5.5mm x 105mm Precontoured Rod

    Ø5.5mm X 105mm PRECONTOURED RODS

    FDA UDI
    XENCO MEDICAL LLC·B064XMPH21511052·

    POWDER-FREE, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEPF1

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BASIS VERTEBRAL BODY SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007303·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    NY-STA BLACK 2/0 18" (45CM) DS24 VPL

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007334·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007341·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007327·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007358·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072007310·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

    WRIST BLOOD PRESSURE UNIT

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, LP - NORTHFIELD·Product code DXN·July 12, 2022

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 6, 2011

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008

    SUPRAMID BLACK 3/0 (2) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023