29 results · 19ms · Sources: EU EUDAMED, US FDA

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Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113225·PS Insert, Size 4 x 11mm

RR - UP - Commuter Passenger - zlb

FDA UDI
Certified Safety Manufacturing, Inc.·00766588024110·RR - UP - Commuter Passenger - zlb

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220411070·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220411150·

X SERIES

FDA UDI
Zoll Medical Corporation·00847946018672·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946005948·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946014896·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220411000·

X SERIES

FDA UDI
Zoll Medical Corporation·00847946019105·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946012601·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946061333·X SERIES, MONITOR/DEFIBRILLATOR, 12 LD W/ INTER...

NUVASIVE TRIAD FACET SCREW SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

Z6/Z60/Z60T/Z60S/Z60 Pro/DP-60 Diagnostic Ultrasound System

FDA 510(k)
FDA Class 2 ·Radiology

VERSACROSS CONNECT LAAC ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

SPECTRUM IQ INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 23, 2022

SPECTRUM IQ INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 13, 2022

SPECTRUM IQ INFUSION PUMP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 25, 2022

K 520411-2, Hercep Test, 35Test, HER2, Protein

FDA Recall
Terminated ·Dakocytomation California Inc·Product code MVC·September 29, 2005

STARCLOSE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·November 4, 2008