BEUDAMED
    28 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 ×

    ATLANTIS Abutment for CONELOG implant

    FDA 510(k)
    FDA Class 2 ·Dental

    ORTHOPEDIC SALVAGE SYSTEM (OSS)

    FDA UDI
    Biomet Orthopedics, LLC·00880304250918·

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707066279·KOBAYASHI PREFORMED WIRE 012"

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16721610300·

    MEGA SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809763500992·Mono Screw Driver

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1672161030060·

    Symmetry Rochester-Pean

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482056028·Symmetry® Forceps, Rochester-Pean Hemostatic, S...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137411·Trial, 30 X 26, 17mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137398·Trial, 30 X 26, 13mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137435·Trial, 30 X 26, 21mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137404·Trial, 30 X 26, 15mm Height 16° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523137428·Trial, 30 X 26, 19mm Height 16° Hyperlordotic

    BIOBLANKET SURGICAL MESH

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

    MODIFICATION TO HBS HEADLESS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·June 17, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    ATLAS REVERSE HUMERAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·September 19, 2018

    BIODESIGN OTOLOGIC REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code KHJ·September 19, 2018

    BIODESIGN OTOLOGIC REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code KHJ·March 8, 2021