28 results · 22ms · Sources: EU EUDAMED, US FDA

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NEOLYNX SCREENING APPLICATION MANAGER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·40677964023727·The ENDO CARRY-ON Procedure Kit contains all of...

KALORE™

FDA UDI
Gc America Inc.·14548161293181·KALORE™ Syringes (2 mL/4 g) B3

KALORE™

FDA UDI
Gc America Inc.·D0470035841·KALORE™ Syringes (2 mL/4 g) B3

SCANLAN® Needle Holders

FDA UDI
SCANLAN INTERNATIONAL INC·00846159026702·Jacobson Needle Holder

METROFOCAL TORIC (HIOXIFILCON A) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBILITY TINT, LATHE-CUT

FDA 510(k)
FDA Class 2 ·Ophthalmic

POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

PF4 IGG

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code LCO·July 1, 2016

TRUSTEEL

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·July 18, 2024

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 2, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

CLEARGLIDE EVH LONGVIEW W/SCIS

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

CLEARGLIDE EVH SMALL W/SCISSOR

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009

CLEARGLIDE EVH LONGVIEW W/SCIS

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2013

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·February 22, 2011