BEUDAMED
    10 results · 17ms · 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.

    INFLATE-A-CUFF #7014

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756019903·FINGER SPLINT

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112359·SURG-I-BAND PURPLE GLOW

    UCR

    FDA UDI
    Seaspine Orthopedics Corporation·10889981080105·Curved Probe

    PTS-X SIZING BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRI-FIX SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 23, 2010

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·POPULAR PLASTICS·Product code IKX·July 2, 2014

    OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM; c) 200-07-32, 32MM; d) 200-07-35, 35MM; e) 200-07-38, 38MM

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·June 26, 2024