BEUDAMED
    257 results · 101ms · 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.

    HERAEUS LASERSONIC, INC STERILE DISPOSABLE FIBERS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HERAEUS LASERSONIC INC. STERILE DISPOSABLE FIBERS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Heraeus Medical Components Caribe, Inc.

    FDA registration
    Heraeus Medical Components Caribe, Inc.·4 products·🇺🇸 United States

    PALACOS R+G BONE CEMENT

    FDA Adverse Event
    Malfunction ·HERAEUS MEDICAL GMBH·Product code LOD·September 29, 2010

    Heraeus Kulzer GLUMA Comfort Bond + Desensitizer light curing one component adhesive, contents: 4 ml, dental bonding agent. Distributed by Heraeus Kulzer, Inc., Armonk, NY; Reorder No. 66001710.

    FDA Recall
    Terminated ·Heraeus Kulzer Inc., Dental Products Division·Product code KLE·July 9, 2007

    Heraeus Kulzer GLUMA Comfort Bond + Desensitizer light curing one component adhesive, Assortment Value Pack 3 x 4 ml, dental bonding agent. Distributed by Heraeus Kulzer, Inc., Armonk, NY; Reorder No. 66018222.

    FDA Recall
    Terminated ·Heraeus Kulzer Inc., Dental Products Division·Product code KLE·July 9, 2007

    PALACOS R BONE CEMENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LOD·October 5, 2012

    PALACOS R+G BONE CEMENT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code LOD·October 17, 2012

    VASCULAR GUIDEWIRE

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code DQX·January 31, 2023

    ANGIODYNAMICS

    FDA Adverse Event
    Injury ·ANGIODYNAMICS, INC·Product code DRE·February 27, 2024

    VASCULAR GUIDEWIRE

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code DQX·January 31, 2023

    ARTGLASS

    FDA Adverse Event
    Malfunction ·HERAEUS KULZER INC.·Product code DZN·December 10, 2002

    PALACOS R+G BONE CEMENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LOD·August 30, 2011

    NEXGEN FLUTED STEM MOBILE TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC.·Product code NJL·March 12, 2013

    NEXGEN STEMMED FLUTED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 23, 2013

    PERSONA CEMENTED STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code JWH·April 7, 2016

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·April 3, 2023

    NEXGEN LPS-FLEX GSF FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 27, 2011

    NATURAL-KNEE FLEX PROLONG PATELLA

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 8, 2015

    *

    FDA Adverse Event
    Malfunction ·HERAEUS INSTRUMENTS INC.·Product code FTD·March 21, 2012