34 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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