7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
DRILL GUIDE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #801116
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LUOFUCON SILVER FOAM DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·May 30, 2014
MX-PRO R-3 AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·October 24, 2012
SILICONE ADVANCED OPTIC LENS
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code HQL·September 16, 2010
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018