BEUDAMED
    22 results · 22ms · 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 ×

    ASCOT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RC Multi-base Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600306368·

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102374·BARRAQUER IRIS SPATULA 0.25MM

    TROUTMAN KATZIN CORNEAL TRANSPLANT SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896014343·TROUTMAN KATZIN CORNEAL TRANSPLANT SCISSORS STR...

    MINI V.A.C., V.A.C. FREEDOM, V.A.C. ATS

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

    WONDFO METHADONE URINE TEST,OPIATE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124190·L Ultracongruent Tibial Insert Trial Sz B 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101979·L CR MAXTM HXL Ultracongruent Tibial Insert Sz ...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523164448·L Ultracongruent Tibial Insert Trial with Anter...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144600·L CR UHMWPE Ultracongruent Tibial Insert Sz B 10mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101115·L CR E-MAXTM Vitamin E Ultracongruent Tibial In...

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017

    GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018

    FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 29, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    CASTVAC W/8 FOOT HOSE AND MOBILE STAND

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code LGH·June 11, 2011