BEUDAMED
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    CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Penrose Drain

    FDA UDI
    C. R. Bard, Inc.·00801741051258·Penrose Drain 12" (304.8mm), X-Ray Opaque Rubbe...

    ENDO-SCRUB®

    FDA UDI
    MEDTRONIC XOMED, INC.·20643169437252·TUBING 1912030 ENDO-SCRUB 2 5PK

    JuggerKnot Soft Anchors

    FDA UDI
    Biomet Orthopedics, LLC·00880304477193·

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112274·SURG-I-BAND WHITE

    Pinnacle

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730010490·Pinnacle 018 Roth U/L 5x5 Hks 3, OS Pad U/L 4/5...

    Pinnacle®

    FDA UDI
    Ortho Organizers, Inc.·00190707112431·Pinnacle .018 Roth U/L 5x5 Hks 3, OS Pad U/L 4/...

    Votion®

    FDA UDI
    Ortho Organizers, Inc.·00190707114367·Votion .018 Roth U/L 5x5 Hks 3, OS Pad U/L 4/5 SPK

    Votion

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730008664·Votion 018 Roth U/L 5x5 Hks 3, OS Pad U/L 4/5 SPK

    PORTABLE INTENSIVE CARE UNIT

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SYNTHES RADIAL HEAD PROSTHESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 7, 2018

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 7, 2018

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 7, 2018

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 7, 2018

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·November 6, 2020

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·November 6, 2020

    JGRKNT SINGLE 1.4MM 1 #1 MB

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·November 6, 2020

    JUGGERKNOT SOFT ANCHORS

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code MBI·September 30, 2024

    CR PROLONG 36MM BRNG +3 RET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·November 2, 2022