22 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPIRA Open Matrix LLIF
FDA 510(k)
FDA Class 2
·Orthopedic
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001117·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001704·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001094·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001698·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001681·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001711·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001674·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001667·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001100·MCK Inlay Tibial Component
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197085953·DESCHAMPS Ligature needle
20.0cm...
GC OPB-100
FDA 510(k)
FDA Class 2
·Dental
OSSEOTITE II MODEL XIFOSSXXX
FDA 510(k)
FDA Class 2
·Dental
MONTERIS MEDICAL NEUROBLATE SYSTEM
FDA Adverse Event
Malfunction
·MONTERIS MEDICAL CORPORATION·Product code GEX·April 22, 2015
BD MICROLANCE¿ 3 NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·October 31, 2019
TRUERESULT
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·October 15, 2014
SCR Ø1.5 SELF-TAP L6 TAN 4U I/CLIP
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWC·June 20, 2013
GEMSTAR 7 SP REFURB
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·May 5, 2011
VIDAS® VARICEL ZOSTER IGG
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LFY·July 17, 2018
ASAHI GLADIUS MG14 PV ES
FDA Adverse Event
Injury
·ASAHI INTECC CO., LTD.·Product code DQX·November 9, 2023