BEUDAMED
    282 results · 21ms · 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 ×

    Longeviti ClearFit Cranial Implant

    FDA 510(k)
    FDA Class 2 ·Neurology

    Orthos

    FDA UDI
    ORMCO CORPORATION·00889989029956·ORTHOS CM SST 017 X 025 UPSM PK10

    Symetri Clear

    FDA UDI
    ORMCO CORPORATION·00889989082913·U2R SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543429·LATERAL IMPLANT TAMP, STOP

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198949·AK3 Congruent Insert Trial Size 2, 10mm

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819121000201·EXMRC MBT 018/UL1 17T 4A

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819121000101·EXMRC ROTH 018/UL1 12T 5A

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107613·TRIAL 90-SRK-191210 POLY-MPCS 2X10 RIGHT

    T:SLIM (TM) INSULIN DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACECIDE-C HIGH LEVEL DISINFECTANT AND STERILANT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025

    CANCELLOUSSCR Ø4 FULL-THR L16 TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KWQ·June 26, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 19, 2011

    RX DILATATION BALLOON

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KOG·September 26, 2008

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026

    INSULIN PUMP

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code LZG·December 2, 2016

    INFUSOMAT®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 3, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025