15 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIMENSION(R) LACTIC ACID METHOD
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ZAVATION
FDA UDI
Zavation LLC·00842166189393·4.5 x 8mm Occipital Screw
MAGNA SURGEONS GOWNS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CONDOR ANALOG INFLATION SYRINGE
FDA 510(k)
FDA Class 2
·Cardiovascular
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO.·Product code LKK·January 14, 2013
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA·Product code LOX·December 3, 2010
PINN SECTOR W/GRIPTION 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 3, 2014