BEUDAMED
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    RADIOPAQUE 7 FRX 12-POLYURETHANE MULTI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONDEAL

    FDA UDI
    MONDEAL Medical Systems GmbH·04050435064036·MCD Screw 4.0 x 36 mm cannulated M3 partia...

    SYNTHES (USA) LATERAL ENTRY FEMORAL NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTIMUS FUSION: SLT, YAG AND YAG/SLT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 30, 2014

    LANKETROL III, HOSE

    FDA Adverse Event
    Malfunction ·CINCINNATI SUB-ZERO PRODUCTS, INC.·Product code DWJ·November 17, 2012

    PATIENT ROOM WALL SAVER RECL

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code FRK·September 10, 2010

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 95MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 105MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018