BEUDAMED
    257 results · 30ms · Sources: EU EUDAMED, US FDA

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    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·CLARIS(TM) REWETTING DROPS

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·WET-N-SOAK(TM) REWETTING DROPS

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·WET-N-SOAK(TM) REWETTING DROPS

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·WET-N-SOAK(TM) REWETTING DROPS

    RMO

    FDA UDI
    Rmo, Inc.·00885797114044·MUSCLE ANCHOR APPL LWR

    Barricade Coil System

    FDA UDI
    BALT USA LLC·00818053020483·Barricade Coil System (BCS) is intended for the...

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746099175·DB BRACKET MASTER SERIES MAND LEFT 1ST BICUSPID...

    ACUMED

    FDA UDI
    Acumed LLC·10806378091353·Total Wrist Fusion Plate X-Ray Template

    CONLIN MOLAR BANDS

    FDA UDI
    Ortho Arch Company Inc·D90990004717·MOLAR BAND CONLIN RX LOWER LEFT 37

    XBraid TT

    FDA UDI
    RIVERPOINT MEDICAL, LLC·00810020085334·Suture Tape

    Palladian™

    FDA UDI
    NEUROSTRUCTURES, INC·00841508106944·Cortical Screw Drill

    THAYER SUCTION EVACUATION CONDENSATE COLLECTION

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 16, 2006

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·ER HEALTHCARE - LARGO·Product code FKX·June 27, 2014

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·January 7, 2013

    P4 28MM 10DEG INSERT OSTEOLOCK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·November 9, 2010

    Wallach LL100 Cryosurgical Freezer No Connector CO2 System Model: 900047.

    FDA Recall
    Terminated ·Cooper Surgical, Inc.·Product code GEH·September 29, 2009