BEUDAMED
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    LECTROSWITCH MODEL E2502B

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

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517658715·Archon Screw, Ø4.5x11mm Self Drill Fix

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77815111·Micro Sprint Bracket McLaugh/Benn/Trev. .022" m...

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77815111001·Micro Sprint Bracket McLaugh/Benn/Trev. .022" m...

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77815110051·Micro Sprint Bracket McLaugh/Benn/Trev. .022" m...

    Micro Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR77815110101·Micro Sprint Bracket McLaugh/Benn/Trev. .022" m...

    2.0 PK SUTURE ANCHOR T, 2.0 PK SUTURE ANCHOR S

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOTAL KNEE PROSTHESIS-NONCONSTRAINED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DELTA CER HEAD 12/14 36MM +5

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·April 30, 2014

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 10, 2012

    TELIGEN 100

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LWS·July 26, 2010

    STERRAD® CYCLESURE® 24 BIOLOGICAL INDICATOR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code FRC·March 24, 2016

    ACCOLADE SR SL MRI (Model L310)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025