BEUDAMED
    40 results · 21ms · 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 ×

    ZEPTO Precision Capsulotomy System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SOLUTION SYSTEM

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295087038·SOLUTION SYSTEM THINSHAFT REAMER 14mm DIA

    PEDICLE SCREW 03.58.225 MUST MC SCREW Ø5X45 CANNULATED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2023

    QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)

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

    COPELAND MB/HA RESURFACING HUMERAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161881·Tribrid LM/RL Baseplate Trial Sz 3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170876·LM/RL TRIBRID Cemented Tibial Baseplate Sz 4

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161904·Tribrid LM/RL Baseplate Trial Sz 5

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170883·LM/RL TRIBRID Cemented Tibial Baseplate Sz 5

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161928·Tribrid Anterior Fixture Offset LM/RL

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161935·Tribrid Tibial Cut Block LM/RL

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170845·LM/RL TRIBRID Cemented Tibial Baseplate Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170852·LM/RL TRIBRID Cemented Tibial Baseplate Sz 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161874·Tribrid LM/RL Baseplate Trial Sz 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161911·Tribrid LM/RL Baseplate Trial Sz 6

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170890·LM/RL TRIBRID Cemented Tibial Baseplate Sz 6

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161867·Tribrid LM/RL Baseplate Trial Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170869·LM/RL TRIBRID Cemented Tibial Baseplate Sz 3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523161898·Tribrid LM/RL Baseplate Trial Sz 4

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·April 9, 2026