22 results · 21ms · Sources: EU EUDAMED, 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