22 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALIF Interfixated System
FDA 510(k)
FDA Class 2
·Orthopedic
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283068·RICHARDSON EASTMAN RETRACTOR 10 1/4" LARGE
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169502154·INTERBODY 2151214 MEDIUM - 6 DEG 14MM
Pro Lift Instruments
FDA UDI
Life Spine, Inc.·00190837031244·
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291229·Knee femur prosthesis trial - Endo Model Knee S...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291243·Knee femur prosthesis trial - Endo Model Knee S...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291205·Knee femur prosthesis trial - Endo Model Knee S...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295475163·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291267·Knee femur prosthesis trial - Endo Model Knee S...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295475156·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295475187·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295475170·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...
ALUMA SKIN RENEWAL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GUARDIAN CONNECTION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·November 18, 2020
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
ARTICULEZE M HEAD 36MM -2
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 30, 2011
DAMON COPPER NITI WIRE
FDA Adverse Event
Malfunction
·ORMCO CORPORATION·Product code DZC·September 9, 2008
OT VERIO FLEX METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015
ACCESS ACCUTNI REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code MMI·September 15, 2016