12 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLES
FDA 510(k)
FDA Class 2
·Ophthalmic
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623942·PEEK Corp Core, Ø14x39mm
EAGLE Plus Anterior Cervical Plate System, EAGLE Plus Micro Anterior Cervical Plate System, PULSE Anterior Cervical Plate System, SKYLINE Anterior Cervical Plate System, SLIM LOC Anterior Cervical Plate System, SWIFT Plus Anterior Cervical Plate System, UNIPLATE Anterior Cervical Plate System, UNIPLATE 2 Anterior Cervical Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
ZIMMER PATIENT-SPECIFIC ABUTMENT, INTERNAL HEX, TITANIUM
FDA 510(k)
FDA Class 2
·Dental
CDS/R/4K DILUENT/SHEATH, 20L
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·April 12, 2007
CD SAPPHIRE, CD 4000 SYSTEMS DILUENT/SHEATH
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·December 8, 2006
CELL-DYN DILUENT/SHEATH
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012
BD VACUTAINER® K2 EDTA (K2E) 10.8 MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 22, 2018
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 31, 2014
EON MINI IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 21, 2011
GE OEC 9900 ELITE
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·October 8, 2007