BEUDAMED
    23 results · 28ms · Sources: EU EUDAMED, US FDA

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    MULTIPLE (ADDITION SILICONE IMPRESSION MATERIAL)

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO OPUS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEVILBISS 9000 SERIES CPAP, MODEL 9001

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118403·PLIF, 22mm X 9mm X 8mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118427·PLIF, 22mm X 9mm X 10mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118465·PLIF, 22mm X 9mm X 14mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118458·PLIF, 22mm X 9mm X 13mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118472·PLIF, 22mm X 9mm X 15mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118489·PLIF, 22mm X 9mm X 16mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118397·PLIF, 22mm X 9mm X 7mm, Convex 5°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118441·PLIF, 22mm X 9mm X 12mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118410·PLIF, 22mm X 9mm X 9mm, Convex 7°, PEEK

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118434·PLIF, 22mm X 9mm X 11mm, Convex 7°, PEEK

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·January 16, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·January 16, 2019

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·January 16, 2019

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 8, 2013

    UNKNOWN ZIMMER ELBOW

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDB·March 30, 2011

    PRECISION LINK

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code NBW·May 8, 2008

    LOGIC TIBIA PS MOD INSRT SZ 3 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 26, 2024