10,000 results · 58ms · Sources: EU EUDAMED, US FDA

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AGEE DIGIT WIDGET

FDA Adverse Event
Malfunction ·HAND BIOMECHANICS LAB, INC.·Product code JDW·December 4, 2017

NAVIAID BGE DEVICE

FDA Adverse Event
Injury ·SMART MEDICAL SYSTEMS LTD.·Product code FDA·July 19, 2009

NAVIAID BGE DEVICE

FDA Adverse Event
Injury ·SMART MEDICAL SYSTEMS LTD.·Product code FDA·September 21, 2008

TRIABEAUTY AGE-DEFYING LASER

FDA Adverse Event
Injury ·TRIA BEAUTY·Product code GEX·April 9, 2014

EPOC BGE TEST CARD

FDA Adverse Event
Malfunction ·EPOCAL INC.·Product code CHL·November 12, 2008

EPOC BGE TEST CARD

FDA Adverse Event
Malfunction ·EPOCAL INC.·Product code CHL·November 12, 2008

EPOC BGE TEST CARD

FDA Adverse Event
Other ·EPOCAL INC.·Product code CHL·November 5, 2009

"NEW SKIN AGE LOC"

FDA Adverse Event
Injury ·Product code GYB·July 9, 2009

ENGAGE INTRODUCER, TF 5 FR 12 CM 0.038 GW

FDA Adverse Event
Injury ·ST. JDE MEDICAL·Product code DYB·November 19, 2010

PMD PERSONAL MICRODERM

FDA Adverse Event
Injury ·AGE SCIENCES INC.·Product code GFE·October 23, 2015

MEDICUBE AGE-R BOOSTER PRO

FDA Adverse Event
Injury ·MEDICUBE/ APR US INC.·Product code ISA·August 28, 2025

MEDICUBE AGE-R BOOSTER PRO

FDA Adverse Event
Injury ·APR CO., LTD·Product code NFO·August 11, 2025

NIRA ANTI-AGING LASER DEVICE

FDA Adverse Event
Injury ·NIRA INNOVATIONS INC.·Product code OHS·October 31, 2024

1.5T HDXT TWINSPEED

FDA Adverse Event
Injury ·HGE MEDICAL SYSTEMS, LLC·Product code LNH·June 24, 2009

INFUSOMAT SPACE - US VERSION

FDA Adverse Event
Malfunction ·B. BRAUN MELSUNGEN AGE·Product code FRN·September 17, 2013

3M AGEE CARPAL TUNNEL RELEASE SYSTEM

FDA Adverse Event
Injury ·MICROAIRE SURGICAL INSTRUMENTS·Product code HRX·April 14, 2000

3M AGEE CARPAL TUNNEL RELEASE SYSTEM

FDA Adverse Event
Injury ·MICROAIRE SURGICAL INSTRUMENTS·Product code HRX·November 15, 1999

NEXTGEN FETAL AGE AND VITAL SIGN SYSTEM

FDA Adverse Event
Injury ·NEXTGEN HEALTHCARE INFORMATION SYSTEM·Product code HGM·March 21, 2014

LUMBR WDG I/F CGE(9X11)X9X23

FDA Adverse Event
Injury ·DEPUY SYNTHES SPINE·Product code MQP·December 26, 2012

LUMBR WDG I/F CGE(9X11)X9X23

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code MAX·May 30, 2018