10 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TORNIER INSITE(TM) FT PEEK KNOTLESS SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131264497·RIA PRO, KIT 312 WL DIR L V BE
ULTRASENSE AF BLUE POWDER-FREE NITRILE EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
QUIDEL MOLECULAR INFLUENZA A+B
FDA 510(k)
FDA Class 2
·Microbiology
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 7, 2024
ETRIO
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 29, 2013
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·May 12, 2011
2520274-2014-01050
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HWE·October 1, 2014
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 11, 2024
Achieva 1.5T
FDA Enforcement
Class II
·Ongoing·Philips North America Llc·November 29, 2023