BEUDAMED
    25 results · 32ms · 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 ×

    PATIENT LATEX POLYMER COATED POWDER-FREE GLOVES, CONTAINS 50 MICROGRAM OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Preat

    FDA UDI
    Preat Corporation·00842092182987·ASC Astra®-compatible 3.0mm Titanium Blank

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002065·artVeneer life lower posteriors, M, B2

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00270651·

    Preat

    FDA UDI
    Preat Corporation·00842092183397·ASC Astra®-compatible 3.0mm – Milled Ti Abutment

    AOS CAPTURED CORTICAL SCREW 4.2mm x 65.0mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019506·

    Silverbolt/Mainframe

    FDA UDI
    Choice Spine, LP·00840996170789·SILVERBOLT,SCREW,POLYAXIAL,5.5X65

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520020650·Curved Cobalt Chrome Rod, Extended Hex

    TAURUS

    FDA UDI
    CTL Medical Corporation·00841732163614·Taurus Pedicle Screw System-Curved Rod Ext Hex ...

    NUTRIENT MIXTURE F-12 (HAM), CAT. #200-2065

    FDA 510(k)
    FDA Class 1 ·Hematology

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252002065·Taurus Pedicle Screw System-Curved Rod Ext Hex ...

    PRIMARY CARE SOLUTIONS STERILE WATER DEVICE IRRIGATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAMLOG CYLINDER IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 13, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 28, 2011

    ENDOSITE XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·VISION SYSTEMS, INC.·Product code GCT·February 19, 2008

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·March 10, 2025

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·August 6, 2025

    REBAR

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·May 12, 2025

    PRESIDIO 10 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2016