BEUDAMED
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    LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS

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

    CSU BALFOUR RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896097797·CSU BALFOUR RETRACTOR MEDIUM SIZE SINGLE BAR SP...

    HS Barr.Burr,Ø4.0x8.0x95,80k

    FDA UDI
    Bien-Air Surgery SA·17630055507515·

    eZ-Fix

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132142608·Nut, Serrated w/Flange

    SURE-LOCK

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828146883·SURE LOCK,A34,10 PK,BLUE LEVER,CURBELL

    CSU BALFOUR RETRACTOR SET

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896088016·CSU BALFOUR RETRACTOR SET SINGLE BAR FENESTRATE...

    Lead Adapter, For use with Multi-Lead Trial Cable to Guideline System

    FDA UDI
    FHC, INC.·00873263006108·Lead Adapter, For use with Multi-Lead Trial Cab...

    APK

    FDA UDI
    APK Technology Co.,Ltd.·06946725503089·ADAPTOR CLIP 10/PACK BLUE LEVER

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100110001·IN-OVATION® C TGO 020X028 U5-5/L3-3 CS-BC HK

    RAPID EXCHANGE BIOPSY CAP AND LOCKING DEVICE #4526 & 4527

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

    RESOLUTION CHOLESTEROL MONITOR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ARCHITECT I1000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·June 23, 2016

    2520274-2013-06104

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·September 6, 2013

    2520274-2013-06119

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 6, 2013

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2013

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2011

    MICRUSFRAME10 5MM X 17CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 4MM X 10CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022

    GALAXY G3 XSFT 4MM X 10CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022