BEUDAMED
    297 results · 25ms · 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 ×

    Arthrex FiberTak Anchors

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BLT Pilot Drill, extra-short

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600304401·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587T1512300·15mm TLIF Implant 12mm Wide 30mm Length

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704283112·DEAVER RETRACTOR HOLLOW 1" X 10"

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192305·Revision Knee Reamer Spiral Fluted - Zimmer 23mm

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587T15123070·15mm TLIF Implant 12mm Wide 30mm Length 7 Degrees

    Flextrode

    FDA UDI
    COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

    NA

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197263764·Millin atraumatic Grasping Forceps for th...

    IPS EMPRESS DIRECT COLOR IPS EMPRESS DIRECT OPAQUE

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES 3.5MM LOW PROFILE CORTICAL SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180161412·Zepli 3” with Ratchet, 90deg, Surgical Grade Au...

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    VERSANAIL 10MMX20CM STERILE

    FDA Adverse Event
    Injury ·DEPUY ACE S.A.'R.L.·Product code HSB·June 30, 2011

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026