47 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ALOKA LISENDO 880
FDA 510(k)
FDA Class 2
·Radiology
BOWMAN LACRIMAL PROBE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896018648·BOWMAN LACRIMAL PROBE SIZE 1/2 ROUND HANDLE STA...
BI-METRIC HEAD/NECK HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304223073·
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHE USA·Product code HWC·April 9, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·September 23, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·September 23, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·October 7, 2015
MUCHECK, VERSION 9.0
FDA 510(k)
FDA Class 2
·Radiology
ELIA CELIKEY IGG WELL, MODEL 14-5518-01, ELIA CELIAC CONTROL, MODEL 83-1011-01
FDA 510(k)
FDA Class 2
·Immunology
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·June 16, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 13, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code HWC·June 2, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 5, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·July 30, 2015
AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 23, 2021
AIRVO TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 18, 2022
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·February 15, 2017
AIRVO2 TUBE AND CHAMBER KIT WITH NEBULIZER ADAPTER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 18, 2022
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012