BEUDAMED
    27 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 ×

    SB ANCHOR

    FDA 510(k)
    FDA Class 2 ·Dental

    ORTHOFIX

    FDA UDI
    ORTHOFIX SRL·18059015374469·STANDARD LOCKING SCREW L60.0MM D4.0MM

    Thermoflect

    FDA UDI
    Encompass Group, L.L.C.·30612899004277·THERMOFLECT JACKET, 2X, 25EA ...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319716175·Foerster Sponge (Ring) Forceps 9-1/2" (23.8cm),...

    ORTHOFIX

    FDA UDI
    ORTHOFIX SRL·18059015373967·STANDARD LOCKING SCREW L60.0MM D4.0MM STERILE

    SureCore Semi-automatic Disposable Biopsy Needle

    FDA UDI
    Canyon Medical Inc.·06954414641387·Semi-automatic Disposable Biopsy Needle

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702254020·Elvarex 2/Thigh High/Slant, Open Toe, E-Version...

    Sterilizable Metal Sleeve

    FDA UDI
    Carl Zeiss Meditec AG·04049539103536·

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702435634·EF3/AG/SL-CT-E/OH-WOV/BR

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167521406000·

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1106000·Tray, Base, 6", Arcamed

    PROSTHODONTIC SCREWDRIVER , MODEL IA-400

    FDA 510(k)
    FDA Class 1 ·Dental

    GENEX BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code QFG·March 1, 2022

    ABVISER AV IAP DEVICE, POLE MOUNT (1X10)

    FDA Adverse Event
    Malfunction ·CONVATEC, INC.·Product code FEN·June 16, 2016

    AEMS V, EMS-1000, MODEL TS-140500 AND AEMS VI, EMS-1000 PLUS, MODEL TS-140600

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    COOLSCULPTING SYSTEM

    FDA Adverse Event
    Injury ·ALLERGAN PLEASANTON·Product code OOK·June 28, 2021

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·May 31, 2013

    LIGASURE ATLAS HANDSWITCHING 37CM

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·June 16, 2011

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·August 28, 2008