BEUDAMED
    9 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 ×

    Panthera Dental Milled Bars

    FDA 510(k)
    FDA Class 2 ·Dental

    BINAXNOW COVID-19 ANTIGEN SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QKP·April 19, 2022

    ARTHREX UNIVERS II SHOULDER PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMITH & NEPHEW INTRADISCAL CATHETER SYSTEM

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

    STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 10, 2020

    BINAX NOW COVID-19 ANTIGEN SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 7, 2022

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 17, 2013

    NONDEHP LS LF PLUMSET-OLCP D-CHAN

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FPA·August 7, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 23, 2011