BEUDAMED
    44 results · 19ms · 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.

    CustomizedBone Service

    FDA 510(k)
    FDA Class 2 ·Neurology

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551058381·BRUENINGS Mastoid Gouge, 15 cm

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM

    SR MCP

    FDA UDI
    Stryker GmbH·00886385020778·S.R. MCP METACARPAL TRIAL, SIZE MD

    PTS PANELS CHOL+HDL+GLU PANEL TEST STRIPS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AMIGO CLASSIC FD

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133703·NSA Cervical Cage, 17.5mm x 15mm x 7mm, 2° Lord...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118335·SA Cervical Cage, 17.5mm x 15mm x 7mm, 7° Lordo...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133772·NSA Cervical Cage, 17.5mm x 15mm x 7mm, 7° Lord...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118199·SA Cervical Cage, 17.5mm x 15mm x 7mm, 2° Lordo...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133505·Assembly, T3 SA Cervical Cage, 17.5mm x 15mm x ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133383·Assembly, T3 SA Cervical Cage, 17.5mm x 15mm x ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120390·17.5mm x 15mm x 7mm 2° Lordotic Trial/Broach w/...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120468·17.5mm x 15mm x 7mm 7° Lordotic Trial/Broach w/...

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

    TDXFLX SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·September 17, 2008

    GREENLIGHT MOXY

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 30, 2011

    Fortilink Cages with TiPlus Technology

    FDA UDI
    Baat Medical Products B.V.·08720246784848·

    Fortilink Cages with TiPlus Technology

    FDA UDI
    Baat Medical Products B.V.·08720246784770·

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019