336 results
·
25ms
·
Sources: EU EUDAMED, US FDA
CARDIMA ABLATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Safco T&F Bur - 12 Bladed
FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310220083·Safco T&F bur - 12 bladed, carbide, #7104 flame...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694000345·2.0mm x 8mm Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694008013·2.0mm x 8mm Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694034814·2.0 x 8mm Lag Screw, Sterile
OsteoMed
FDA UDI
OSTEOMED LLC·00845694028745·2.0mm x 8mm Screw, Sterile
K032008
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054317·2.0 x 8mm Screw Sterile Qty 10
OsteoMed
FDA UDI
OSTEOMED LLC·00845694066402·HPS 2.0 x 8mm Lag Screw Sterile Qty 5
SURGICAL DYNAMICS SPINAL RETRACTOR
FDA 510(k)
FDA Class 2
·Orthopedic
STS RANGE , MODELS STS20,STS30,STS40
FDA 510(k)
FDA Class 2
·Cardiovascular
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·October 17, 2008
ENDO STITCH 10MM SUTURING DEVICE
FDA Adverse Event
Malfunction
·NORTH HAVEN - USS·Product code MFJ·May 2, 2008
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·October 2, 2008
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH LTD / HUNTINGTON·Product code HQL·June 20, 2008
AUTOSONIX ULTRA SHEARS LONG
FDA Adverse Event
Malfunction
·NORTH HAVEN - USS·Product code LFL·December 2, 2008
XENFORM
FDA Adverse Event
Other
·TEI BIOSCIENCES INC.·Product code FTM·June 28, 2013
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH LTD./HUNTINGTON·Product code HQL·May 23, 2008
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH LTD./HUNTINGTON·Product code HQL·May 23, 2008
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·September 5, 2008