BEUDAMED
    53 results · 24ms · 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 ×

    RECLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0012

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

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033183·Baltic Denture System BDLoad BDLoad ↓ Mw7 PLSEu...

    MEDRAD STELLANT CT INJECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THERMAGE THERMACOOL II SYSTEM

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

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 2, 2022

    LOGIC TIBIA PS MOD INSRT SZ 3 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 2, 2022

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 23, 2022

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 3, 2013

    SAGITTAL ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER·Product code GFA·February 28, 2011

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·April 23, 2008

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 4, 2022

    LOGIC TIBIA PS MOD INSRT SZ 4 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 3, 2024

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 10, 2023

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 10, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·March 5, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 9, 2024

    LOGIC FEMORAL PS CEM RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 21, 2024