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

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    Irrisept Wound Debridement and Cleansing System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Nucleus

    FDA UDI
    COCHLEAR LIMITED·09321502017787·Cochlear Nucleus CP800 Series Compact Rechargea...

    36M - Salt River Project-31 - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588022024·36M - Salt River Project-31 - Metal

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113325·PHACO KNIFE 2.8MM ANGLED (BX/5)

    RD-2104

    FDA 510(k)
    FDA Class 2 ·Dental

    LAMITRODE S-SERIES (S4 AND S8) LEADS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102105·R Tibial Baseplate Cemented Keeled Sz 3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102082·R Tibial Baseplate Cemented Keeled Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102075·R Tibial Baseplate Cemented Keeled Sz 0

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102150·R Tibial Baseplate Cemented Keeled Sz 8

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102136·R Tibial Baseplate Cemented Keeled Sz 6

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102143·R Tibial Baseplate Cemented Keeled Sz 7

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102099·R Tibial Baseplate Cemented Keeled Sz 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102112·R Tibial Baseplate Cemented Keeled Sz 4

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102129·R Tibial Baseplate Cemented Keeled Sz 5

    RENOVIS

    FDA Adverse Event
    RENOVIS SURGICAL TECHNOLOGIES·Product code JWH·October 26, 2016

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 22, 2025

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 14, 2026

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 28, 2013

    CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNT·October 16, 2008