BEUDAMED
    7,928 results · 30ms · 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 ×

    Integra®

    FDA UDI
    INTEGRA LIFESCIENCES CORPORATION·10381780251446·Integra® Keller Depth Gauge

    KDG Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    KDG ACETABULAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Radian MIS Bunion System

    FDA UDI
    NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810005669238·Instrument: K-Wire Depth Gauge. The Radian MI...

    BOXED CHISEL

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KDG·October 15, 2014

    BOXED CHISEL

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KDG·December 10, 2014

    BOX CHISEL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code KDG·December 8, 2008

    ACUFEX, MOSAIC PLASTY-TUBULAR CHISEL 3.5MM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Product code KDG·May 24, 1999

    DEVICE ONE: CERVICAL INSTRUMENT CHISEL, 7MM

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code KDG·April 22, 2013

    ACUFEX MOSAICPLASTY 4.5MM TUBULAR CHISEL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KDG·August 20, 1997

    ACCUFEX

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code KDG·April 4, 1997

    ACUFEX MOSAIC PLASTY-TUBULAR CHISEL 3.5MM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIV.·Product code KDG·April 4, 1997

    KONIG 9" (22.9 CM) STRAIGHT LAMBOTTE OSTEOTOME WITH 6 MM BLADE

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code KDG·October 14, 2020

    RD INSTRUMENT INTRADISCAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KDG·April 22, 2024

    UNKN ORTHOPAEDIC RECONSTRUCTION DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KDG·November 26, 2021

    WECK SYSTEMS

    FDA Adverse Event
    Malfunction ·WECK SYSTEMS·Product code KDG·May 7, 2003

    OSTEOTOME

    FDA Adverse Event
    Malfunction ·Product code KDG·July 24, 2012

    PROXIMATE HCS HEMORR CIR STAPL

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KDG·July 22, 2005

    LEXER CHISEL 8.0/ 1.280

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KDG·November 12, 2013

    BOX CHISEL

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code KDG·August 19, 2010