BEUDAMED
    23 results · 20ms · 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.

    MTM(R) CLEAR ALIGNER

    FDA 510(k)
    FDA Class 2 ·Dental

    NexxZr™ T / D-100-12-NT-D200-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113559·

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981192907·Interbody, 11mm x 32mm x 14mm, 15 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981208011·Trial, 11mm x 32mm x 14mm, 15 deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981204747·Trial, 11mm x 32mm x 14mm, 15 Deg

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981288891·Interbody, 11mm x 32mm x 14mm, 15 Deg, 3D

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981190590·Interbody, 11mm x 32mm x 14mm, 15 Deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981200893·Interbody, 11mm x 32mm x 14mm, 15 deg

    BINAXNOW COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·April 18, 2022

    AUDICOR UPGRADE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MS33I2

    FDA 510(k)
    FDA Class 2 ·Radiology

    AMISTEM H CEMENTLESS STEM #3 STD

    FDA Adverse Event
    Injury ·Product code LZO·June 19, 2015

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2015

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2015

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·October 1, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 17, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    STM PROTECTOR

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·March 3, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 30, 2013

    CELL-DYN SAPPHIRE ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·July 17, 2007