BEUDAMED
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    OPTIMA CT520

    FDA 510(k)
    FDA Class 2 ·Radiology

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011123596000·Super hard metal burs, with cross toothing cut,...

    TOTAL KNEE REPLACEMENT CEMENT KLASSIC TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·TOTAL JOINT ORTHOPEDICS, INC.·Product code JWH·August 18, 2020

    WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDRAD 8-RECEIVER PHASED ARRAY NEUROVASCULAR COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·March 4, 2015

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·May 17, 2013

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·September 26, 2014

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2011

    Stryker Howmedica Osteonics; Stryker T2 Humerus System Teflon Tube, sterile; REF 1806-0073S The T2 Nailing System is designed to treat complex fractures in Humeral, Femoral, Tibial and Ankle applications. The Teflon Tube is an optional instrument used to exchange the Ball Tip Guide Wire with the Smooth Tip Guide Wire once reaming is completed. Stryker Stryker Trauma GmbH 24232 Schonkirchen, Germany distributed in USA by: Howmedica Osteonics Corp., 235 Corporate Drive,

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·January 2, 2013