BEUDAMED
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    ORTHOPILOT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Premier Elevator

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783003963·ELEVATOR-LUXATING 3 STRAIGHT

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040060893·CSR Wrap 12"x12"

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040007518·CSR Wrap 12"x12"

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099860·MN 2ND BI BD KT N/L R/L 176

    COOLTOUCH II

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

    MERIDIAN-II AND MERDIAN-PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    INSET I

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 5, 2025

    iQ200

    FDA UDI
    BECKMAN COULTER IRELAND INC.·10837461001317·"iQ200 Select 2008 Instrument; 800-7190 IRICELL...

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 4, 2016

    2520274-2013-10929

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NKB·February 28, 2013

    VORTX 18 FIBERED PLATINUM COIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code KRD·March 1, 2011

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Other ·STAAR SURGICAL CO.·Product code HQL·February 27, 2008

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 23, 2012

    INSET I

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 6, 2025

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·November 11, 2025

    QUICKSET ACE GRATER HEAD 45MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·January 9, 2016

    QUICKSET ACE GRATER HEAD 45MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·April 28, 2016

    QUICKSET ACE GRATER HEAD 36MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·April 21, 2016

    QUICKSET ACE GRATER HEAD 46MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·April 28, 2016