301 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Amendia Interbody Fusion Devices
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517637925·CoRoent Ant TLIF PEEK, 15x11x32mm 12°
Flextrode
FDA UDI
COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G
NA
FDA UDI
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043850·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 22X110MM
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043881·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 22X160MM
ATTUNE
FDA UDI
DEPUY (IRELAND)·10603295043843·ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 22X60MM
JOINSOON ELECTRONICS MFG CO., LTD INFRARED EAR THERMOMETER, MODEL TT-001
FDA 510(k)
FDA Class 2
·General Hospital
PNEUPAC VRI STANDARD, MODEL VRISTDNUS, PNEUPAC VRI RESPONDER, MODEL VRIRESNUS
FDA 510(k)
FDA Class 2
·Anesthesiology
STAR
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code LZS·October 8, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 7, 2013
GPS PROCEDURAL STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·June 7, 2011
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026