BEUDAMED
    48 results · 57ms · 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.

    ALTO DEVELOPMENT CORP.

    FDA registration
    ALTO DEVELOPMENT CORP.·13 products·🇺🇸 United States

    A&E MEDICAL MYOWIRE IIA&E MEDICAL MYOWIRE II

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP·Product code GAO·July 22, 2015

    MYO/WIRE II

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP.·Product code GAQ·September 25, 2003

    PACING WIRE

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP.·Product code LDF·April 4, 2000

    A&E MEDICAL ELECTROSURGICAL PENCIL

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP.·Product code GEI·October 30, 2008

    SUCTION COAGULATOR

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP.·Product code GEI·July 18, 2014

    ILLUMINATED DIRECT VIEW RETRACTOR

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP·Product code GAD·December 13, 2005

    MYO/WIRE II

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP·Product code GAQ·December 27, 2001

    WIRE TWSITER

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP.·Product code HXS·November 15, 2016

    MYO/WIRE

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP.·Product code LDF·February 23, 2005

    MYO/WIRE

    FDA Adverse Event
    Death ·ALTO DEVELOPMENT CORP.·Product code LDF·March 12, 1998

    MYO/PUNCH ROTATING SURGICAL PUNCH

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP·Product code LRY·November 1, 2013

    STERNAL NEEDLE DOUBLE WIRE BALL.CS#3.USP#6.65MM

    FDA Adverse Event
    Malfunction ·AE MEDICAL / ALTO DEVELOPMENT CORP.·Product code GAO·April 22, 2022

    MYO/WIRE

    FDA Adverse Event
    Injury ·ALTO DEVELOPMENT CORP. A&E MEDICAL·Product code LDF·June 20, 1997

    A&E MEDICAL 4.0 ROTATING SURGICAL PUNCH

    FDA Adverse Event
    Injury ·A&E MEDICAL / ALTO DEVELOPMENT CORP.·Product code LRY·December 22, 2020

    STERNALOCK XP RIGID FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET/ALTO DEVELOPMENT CORP.·Product code HRS·June 17, 2024

    ZIMMER BIOMET STERNALOCK XP RIGID FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP./A&E MEDICAL CORP.·Product code IKD·September 22, 2025

    STERNALOCK X RIGID FIXATION SYSTEM IMPLANT X CABLE PLATE

    FDA Adverse Event
    Malfunction ·A&E MEDICAL CORP./ALTO DEVELOPMENT CORP.·Product code HRS·May 16, 2025

    MYO/WIRE

    FDA Adverse Event
    Injury ·A&E MEDICAL CORP./ALTO DEVELOPMENT CORP.·Product code IKD·March 25, 2026

    MYO/WIRE II

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP, DBA A&E MEDICAL·Product code GAO·January 28, 2013