BEUDAMED
    30 results · 37ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    PROCLEAR TORIC XR, PROCLEAR MULTIFOCAL XR, PROCLEAR MULTIFOCAL TORIC, PROCLEAR SPHERE & ASPHERE, TORIC CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517636065·CoRoent Ant TLIF PEEK, 11x12x30mm 12°

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526749740·MANUMED RFX FRACTURE BRACE, RIGHT SIZE 2

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902097805·DISTRACTOR 9112302 16MM CYLINDER SHAFT

    Baby Gorilla/Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795035059·MTP Spin Guard Female Reamer Protector Sleeve, ...

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·August 8, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 2, 2022

    MYLABSEVEN, MYLABALPHA

    FDA 510(k)
    FDA Class 2 ·Radiology

    ADHESIVE EXL-759

    FDA 510(k)
    FDA Class 2 ·Dental

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200070·7mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200090·9mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200130·13mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200120·12mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200140·14mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200080·8mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200110·11mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230200100·10mm LG FP Lordotic Implant, HiJAK™ Stand Alone

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 14, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 23, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·May 24, 2011