10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DynaClip Bone Staple
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517639516·CoRoent Ant TLIF PEEK, 9x13x30mm 15°
AGXO
FDA UDI
Oticon A/S·05707131341464·G200, BTE 13 2.4G 85 C092 AGXO
PENUMBRA EMBOLIZATION COIL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
ENHANCED ULTRA VIT PROBE
FDA 510(k)
FDA Class 2
·Ophthalmic
SYNERGY¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 4, 2015
RADIFOCUS GLIDEWIRE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 7, 2008
PINNACLE PELVIC FLOOR REPAIR KITS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013
SUPERLINE
FDA Adverse Event
Injury
·DENTIUM USA·Product code DZE·July 25, 2011
PEDICLE SCREW 03.50.054 PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·June 16, 2023