38 results · 25ms · Sources: EU EUDAMED, US FDA

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Accusil Dental Impression Materials (Accusil Light Body Regular and Fast Set, Accusil Heavy Body Regular and Fast Set, Accusil Monophase Regular and Fast Set, Accusil Putty Regular and Fast Set, Accusil Bite Registration)

FDA 510(k)
FDA Class 2 ·Dental

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777464·LUMBAMED PLUS FLEX PAD WM SILVER IV

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668114230·LASIK CANNULA FORMS 27GA 4-PORTS

COMFORTCARE COMPRESSION SUPPORT WITIH MAGNETS AND AEGIS MICROBE SHIELD COMFORTCARE MAGNETIC INSOLES AND AEGIS MICROBE

FDA 510(k)
FDA Class 1 ·General Hospital

SYNAPSE MPR FUSION

FDA 510(k)
FDA Class 2 ·Radiology

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·March 25, 2025

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·March 25, 2025

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·March 25, 2025

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 18, 2021

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·June 22, 2025

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·December 23, 2025

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·January 5, 2026

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·January 5, 2026

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 18, 2021

BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 18, 2021

AVOSET INFUSION PUMP ROW

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FRN·April 29, 2026

ARTICULEZE M HEAD 36MM +1.5

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·August 12, 2011

CORE SUMEX DRILL

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·October 30, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 9, 2013

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 22, 2024