36 results
·
24ms
·
Sources: EU EUDAMED, US FDA
EYEFEEL OPHTHALMIC WARMER
FDA 510(k)
FDA Class 1
·Physical Medicine
S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GENZYME DIRECT-AMYLASE TEST REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
UNKNOWN COPELAND SHOULDER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HSD·April 14, 2017
COPELAND SH HUM SZ4 STND PLUS
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HSD·June 8, 2016
UNKNOWN COPELAND HEMIARTHROPLASTY SHOULDER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HSD·October 21, 2016
UNKNOWN COPELAND RESURFACING SHOULDER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HSD·May 16, 2017
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 26, 2013
TERUMO CDI 540 CALIBRATOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·February 25, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·March 28, 2008
UNKNOWN COPELAND SHOULDER GLENOID COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HSD·July 5, 2017
FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·October 18, 2017
CONTIMUUM LINER IT ALLOFIT ACETABULAR SYSTEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWZ·October 18, 2017
SHELL WITH MULTI HOLES POROUS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·October 18, 2017
BONE SCREW SELF-TAPPING
FDA Adverse Event
Death
·ZIMMER MANUFACTURING B.V.·Product code JDI·July 24, 2017
FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·July 24, 2017
BONE SCREW SELF-TAPPING
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JDI·July 24, 2017
BONE SCREW SELF-TAPPING
FDA Adverse Event
Death
·ZIMMER MANUFACTURING B.V.·Product code JDI·July 24, 2017
CONSTRAINED LINER WITH CONSTRAINING RING
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWZ·July 24, 2017
BONE SCREW SELF-TAPPING
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JDI·July 24, 2017