BEUDAMED
    19 results · 20ms · Sources: EU EUDAMED, US FDA

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    Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193101828·EVOS Straight HA PEEK 15mm x 11mm x 30mm Flat, ...

    Symmetry Cone

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001226·Symmetry® Curette, Cone Ring, Straight, Size 3,...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776154950·Switching Stick 10mm x 38cm (15"), Blunt Rounde...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981247300·No-Profile Interbody, 39mm x 30mm x 10mm, 15 Deg

    Lumbar IBFD

    FDA UDI
    KEOS·B084KPS22310150·

    Lumbar IBFD

    FDA UDI
    KEOS·B084KPS12310150·

    Advantage Plus Cage Inserter

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215067908·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197122498·Capener Osteotome curved...

    BIODESIGN ONLAY DURAL GRAFT OR BIODESIGN DURAPLASTY GRAFT

    FDA 510(k)
    FDA Class 2 ·Neurology

    EMBRYOGLUE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369313·PEARSON ATTACHMENT - BRADY

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981331023·Lollipop Trial, Anterior-Angled, 23mm x 10mm x ...

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981441470·Lollipop Trial 23mm x 10mm x 55mm, 15°

    The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent framework. The inner lumen of the covered stent is carbon impregnated.

    FDA Enforcement
    Class II ·Ongoing·Bard Peripheral Vascular Inc·February 15, 2023

    POSTERIOR CHAMBER INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·October 28, 2008

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·July 19, 2011

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2013

    BD NEEDLE 18X1-1/2 RB TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·May 6, 2024