BEUDAMED
    138 results · 23ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Axcent Acrylics

    FDA UDI
    GARRECO, LLC·D79330103200·Repair DK FIB 20lb

    ACP

    FDA UDI
    Nuvasive, Inc.·00887517061713·ACP 2.1H Plate, 22mm 1-Level

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890103200·Zirlux Titanium Screw compatible with: Dentsply...

    Oxygen Sensor

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043103203·

    AOS MODULAR NAIL 10.0mm x 32cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665003000·

    Soft-Form™ ALD External Nasal Splint

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501022502·Soft-Form™ ALD External Nasal Splint, Large

    SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SONOS AIRES 600 (SA-600)

    FDA 510(k)
    FDA Class 2 ·Radiology

    GEN2 ADJUSTABLE GASTRIC BAND - 11 CM, UNLOCKA

    FDA Adverse Event
    Malfunction ·OBTECH MEDICAL SARL_·Product code LTI·March 19, 2013

    4.0MM 6 FLUTE ROUND BUR - HOLLOW, FORMULA (5BX)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code HRX·February 11, 2011

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    LOGIC FEMORAL PS CEM RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 21, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 2, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 16, 2024

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 26, 2019

    LOGIC TIBIA PS MOD INSRT SZ 2 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 28, 2024

    LOGIC TIBIA PS MOD INSRT SZ 2 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2019

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2025

    KNEE IMPLANT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 16, 2024