9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA
FDA 510(k)
FDA Class 2
·Orthopedic
AQUA-PAD FOR MOIST OR DRY HEAT THERAPY
FDA 510(k)
FDA Class 2
·Physical Medicine
T4 CLASP-BEAD EIA KIT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·July 6, 2018
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·July 6, 2018
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·July 6, 2018
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·June 26, 2014
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·November 11, 2010
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 28, 2012