BEUDAMED
    32 results · 23ms · 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 ×

    KC200, SURGICAL MASK, KC200, PROCEDURE MASK, KC300, SURGICALMASK, FLUIDSHIELD, KC300, PROCEDURE MASK, FLUIDSHIELD MODEL

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

    SureFISH RET BA P20

    FDA UDI
    AGILENT TECHNOLOGIES, INC.·05700574009465·SureFISH RET BA P20

    TMA - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989028867·BRD ARCH LOFRIC.TMA LOSM 016X022 PK10

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481118401·LOCATOR R-Tx Abutment For, Syra Ø4.1mm Implants...

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471156209·Cutanium 27° D-Form 013

    DENALI® Spinal System

    FDA UDI
    VB Spine LLC·10888857528321·Tap Size Ø5.5 mm

    BIOPSY SITE MARKER

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

    BIODESIGN NIPPLE RECONSTRUCTION CYLINDER

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

    TMA Archwires, Part Number 211-1402, Lot Number 10K291, Product Description and Intended Use: The intended use of this device is an archwire during orthodontic treatment.

    FDA Recall
    Terminated ·Ormco Corporation·Product code DZC·March 15, 2011

    PRONTO SPOT CHECK PULSE CO-OXIMETER

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·July 9, 2018

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 7, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 23, 2014

    UNKNOWN PEGS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HRS·May 13, 2011

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·December 23, 2021

    LOGIC CR TIB INSERT SLOPE++, SZ 3, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·January 11, 2022

    LOGIC CR TIB INSERT STD, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 2, 2022

    LOGIC CR TIB INSERT STD, SZ 1.5, 9 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 10, 2025

    LOGIC CR TIB INSERT SLOPE ++, SZ 3.5, 13 MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 18, 2024

    LGC TIBIAL FIT TRAY CEM SZ 4F / 4T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024