29 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TITANIUM CEMENT RESTRICTOR MATERIAL PLDLA
FDA 510(k)
FDA Class 2
·Orthopedic
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964150807·Endo Carry-on Procedure Kit contains Basin, Spo...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450129142·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170809·
Matira
FDA UDI
Kalitec Direct LLC·B073DRK010029·Drill Guide, Variable, Attached Handle
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170847·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170816·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170823·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170830·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170854·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07310K0100290·Caddie Lid, MIS Rods and Caps
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033170793·
LIFESTYLE MV2 (TM) TORIC (POLYMACON) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR (CLEAR OR TINTED)
FDA 510(k)
FDA Class 2
·Ophthalmic
POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELLING CLAIM, CONTAINS 50 MICROGRAMS OR LESS OF TOTA
FDA 510(k)
FDA Class 1
·General Hospital
LAMITRODE S8
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 14, 2013
NATURAL HIP SYSTEM TAPER CEMENTED STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·March 1, 2011
*
FDA Adverse Event
Malfunction
·SKYTRON·Product code FQO·February 6, 2008
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·December 22, 2011