BEUDAMED
    9 results · 23ms · 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 ×

    KARL STORZ INSTRUMENTS FOR BIPOLAR COAGULATION

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

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746091667·DB BRACKET LP MAX LEFT CUSPID 020X020 V-SLOT 02...

    OMNI Knee

    FDA UDI
    Omni Life Science, Inc.·00841690101635·Ultra Tibial Insert CS, Size 3 x 16mm

    ACUFEX SUTURE RETRIEVER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    THOMAS MEDICAL BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·March 12, 2025

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 13, 2010

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·January 30, 2013

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·July 15, 2014