BEUDAMED
    14 results · 19ms · 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.

    SLEEP SPLINT

    FDA 510(k)
    FDA Class 2 ·Dental

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040119683·NITINOL RIGHT FORM NATURAL ARCHWIRE .014 LOWER

    Dr. Ronald Jordan Composite Instrument Series REJ #22

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883003005·Dental restorative material applicator

    Dr. Ronald Jordan Composite Instrument Series REJ #22

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172001090·Dental restorative material applicator

    SCOTT'S SELECT GENERAL PURPOSE CLEANER LIQUID 1 GAL

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77810601220·GENERAL PURPOSE CLEANER (1/pack) Volume: 1 gall...

    COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONTINUOUS FLOW Y-TUBING

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KENTROX SL-S 65/16

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO·Product code LWS·July 21, 2006

    DESARA BLUE TV

    FDA Adverse Event
    Injury ·CALDERA MEDICAL INC.·Product code OTN·December 5, 2019

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 20, 2013

    EASYTRAK

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·April 15, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 10, 2008

    NEILMED SINUS RINSE

    FDA Adverse Event
    Injury ·NEILMED PHARMACEUTICALS, INC.·Product code KCJ·January 23, 2024

    NEILMED SINUS RINSE

    FDA Adverse Event
    Injury ·NEILMED PHARMACEUTICALS, INC.·Product code KCJ·January 23, 2024