15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION OF PURESPERM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984172·anteriors; shade A3.5; mould 95
ACCUPLACE (TM)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MODIFIED OLSEN #770 DISPOSABLE HOLSTER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 13, 2013
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·January 8, 2014
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 12, 2015
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 6, 2012
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 24, 2013
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·April 1, 2013
COULTER® LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·February 28, 2013
SOFTCLIX® LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·February 10, 2011
SUPER SUCKER SHORT (BX/20)
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013
SMART PORT CT
FDA Adverse Event
Malfunction
·ANGIODYNAMICS·Product code LJT·September 26, 2024