BEUDAMED
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    2.4mm X 127 cm Phoenix Atherectomy Deflecting System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Globe Scientific

    FDA UDI
    GLOBE SCIENTIFIC INC.·00840095620314·Pipette tip, 0.1-20uL, natural universal, 45mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192398·Apex Revision Knee Reamer – ZIMMER LONG FLUTES,...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694046800·PrimaLIF LLIF PEEK Implant, 11mm X 18mm X 45mm,...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304004·Orthopaedic implant inserter/extractor, reusabl...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304110·Orthopaedic implant inserter/extractor, reusabl...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575303991·Orthopaedic implant inserter/extractor, reusabl...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304028·Orthopaedic implant inserter/extractor, reusabl...

    Statcorp Medical

    FDA UDI
    Statcorp Medical·10841522123412·BP CUFF,TL YLW VNYL,1T,ADULT,26-35CM,HP,5/BG

    Statcorp Medical

    FDA UDI
    Statcorp Medical·10841522104510·BP CUFF,TL YLW VNYL,1T,ADULT,26-35CM,HP, EA

    CRITIVIEW

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250

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

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

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

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·January 6, 2003

    OT VERIO IQ METER

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

    HIP HEAD,10/12 TAPER,28MM,+5MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 30, 2011

    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

    SKIN SUTURE PACK DAFILON

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 18, 2024