8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Tritanium X PL Expandable Posterior Lumbar Cage, Tritanium X TL Expandable Curved Posterior Lumbar Cage
FDA 510(k)
FDA Class 2
·Orthopedic
BD ORIGINAL PEN NEEDLE
FDA Adverse Event
Injury
·BD·Product code FMI·January 25, 2013
NITRILE CORNFLOWER BLUE POWDER-FREE EXAMINATION GLOVES WITH TESTED FOR USE WITH CHEMOTHERAPY DRUG LABELING CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
QUICKIE RHYTHM
FDA 510(k)
FDA Class 2
·Physical Medicine
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 17, 2014
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 21, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·July 28, 2011
Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant only. The AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment. Part number: V000172
FDA Enforcement
Class II
·Terminated·Vision RT Ltd·October 10, 2018