BEUDAMED
    50 results · 21ms · Sources: EU EUDAMED, US FDA

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    Mectaplug PE II

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

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010101709·STAINLESS STEEL INSIDE CALIPERS 174.6MM

    Vessel Probe 15cm 1.5mm, thin wire blue alu handle

    FDA UDI
    Geister Medizintechnik GmbH·04057034046005·Vessel Probe 15cm 1.5mm, thin wire blue a...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319721681·McKenty Septum Elevator 5-1/2" (13.8cm), curved...

    Salvo® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642174649·9.5 x 65 mm Bone Screw, Cannulated, 3 mm Pitch

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304210455·

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L21006224K0·Hex Driver

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L21006219K0·Hex Driver

    GLOBAL UNITE

    FDA UDI
    DEPUY (IRELAND)·10603295451716·GLOBAL UNITE FX REVERSE SHOULDER ARTHROPLASTY C...

    GLOBAL UNITE

    FDA UDI
    DEPUY (IRELAND)·10603295451709·GLOBAL UNITE FX REVERSE SHOULDER ARTHROPLASTY C...

    Dilator, Vascular, acc. Geister 15cm 1.5mm alu-handle BLUE

    FDA UDI
    Geister Medizintechnik GmbH·04057034046029·Dilator, Vascular, acc. Geister 15cm 1...

    STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG

    FDA 510(k)
    FDA Unclassified ·Unknown

    EXPLOR 12X24 MM IMPLANT HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·March 17, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 22, 2024

    EXPLOR MODULAR RADIAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·March 12, 2025

    PENCAN SPINAL TRAYS

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL, INC.·Product code CAZ·June 27, 2013

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code MAX·August 12, 2011

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code LFL·October 22, 2008

    ExploR 7x26mm Modular Radial Stem, Catalog number 11-210062. Elbow prosthesis orthopedic implant.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·May 21, 2014