34 results · 23ms · Sources: EU EUDAMED, US FDA

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ASP TITANIUM

FDA 510(k)
FDA Class 2 ·General Hospital

RESPONSE 2000 HIP STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ATHENA REMOTE CONTROLLED RF SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

3004068499-2017-00003

FDA Adverse Event
Malfunction ·February 10, 2017

3004068499-2017-00001

FDA Adverse Event
Malfunction ·February 10, 2017

3004068499-2017-00002

FDA Adverse Event
Malfunction ·February 10, 2017

3004068499-2017-00004

FDA Adverse Event
Malfunction ·February 10, 2017

INTRALASE FS2

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·November 21, 2013

SPS-1

FDA Adverse Event
Malfunction ·ORGAN RECOVERY SYSTEMS, INC.·Product code KDL·January 30, 2017

SPS-1

FDA Adverse Event
Injury ·ORGAN RECOVERY SYSTEMS·Product code KDL·December 22, 2016

SPS-1

FDA Adverse Event
Malfunction ·ORGAN RECOVERY SYSTEMS·Product code KDL·January 24, 2017

SPS-1 (HTTP://WWW.ORG-AN-RECOVERY)

FDA Adverse Event
Injury ·ORGAN RECOVERY SYSTEMS·Product code KDL·December 22, 2016

VISX EXCIMER LASER

FDA Adverse Event
Injury ·AMO MANUFACTURING USA LLC·Product code LZS·November 5, 2010

INTRALASE FS2

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·August 20, 2013

SPS-1

FDA Adverse Event
Malfunction ·ORGAN RECOVERY SYSTEMS·Product code KDL·December 23, 2016

SPS-1

FDA Adverse Event
Injury ·ORGAN RECOVERY SYSTEMS·Product code KDN·February 2, 2017

INTRALASE FS2

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·October 30, 2013

SPS-1

FDA Adverse Event
Malfunction ·ORGAN RECOVERY SYSTEMS, INC.·Product code KDL·January 30, 2017

COMPR 12MM IM HMRL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBF·April 1, 2019

ORGAN PRESERVATION SOLUTION SPS

FDA Adverse Event
Malfunction ·ORGAN RECOVERY SYSTEMS·Product code KDL·December 22, 2016