BEUDAMED
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    POMERANTZEFF EQUATOR PLUS CAMERA

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Renovis S141 Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMBI 8 MAX

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    STYLE 115 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 7, 2026

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code MCX·April 24, 2014

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 12, 2007

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·October 3, 2012

    Model 6149 Pacing Vector Selector Cable Switch for use with Pacing System Analyzers * Rx only * Contents Are Not Sterile * Manufactured by Remington Medical Incorporated, 6830 Meadowridge Court, Alpharetta, GA 30005, (770) 888-8520 or (800) 999-0057 * Distributed By: Guidant Corporation, 4100 Hamine Avenue North, St. Paul, MN 55112-5798 USA.

    FDA Recall
    Terminated ·Remington Medical Inc.·Product code DTA·August 31, 2005

    Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)

    FDA Recall
    Terminated ·Remington Medical, Inc.·Product code KNW·December 2, 2022