BEUDAMED
    43 results · 20ms · 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 ×

    PROPHECY INBONE PRE-OPERATIVE NAVIGATION ALIGNMENT GUIDES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169601284·SPACER 2110360 OLIF25 20MM 0 DEG 12X60

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517573988·CoRoent Ant TLIF Ti, 11x10x36mm 0°

    AOS TIBIAL NAIL 10mm x 36.0cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016154·

    Luxatemp® Automix Solar

    FDA UDI
    DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG1103600·Dual cure temporary crown and bridge material a...

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529581183·Apex Femoral Nail PF Left Ø 11.0 x 360mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529584689·Apex Tibial Nail Ø 11 x 360mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529588045·Apex Femoral Nail Retrograde Ø 11.0 x 360mm

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306816123·Mayo-Adams Retractor, 2 Blades, 17cm

    NATRELLE Silicone-Filled Breast Implants

    FDA UDI
    Allergan, Inc.·10888628002241·NATRELLE Style 110-360 Moderate profile BIOCELL...

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585242·Apex Femoral Nail PF Right Ø 11.0 x 360mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586140·Apex Femoral Nail GT Left Ø 11.0 x 360mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587048·Apex Femoral Nail GT Right Ø 11.0 x 360mm

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    KENSTONE METAL·Product code ITJ·July 20, 2012

    BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BEL-CYPHER N

    FDA 510(k)
    FDA Class 2 ·Dental

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 6, 2015

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 20, 2016

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016