24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Rhino-Laryngo Fiberscope Olympus ENF-GP2
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704512649·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515025288·Kocher Ret, 18mm wide, 40mm deep
Regatta Lateral System
FDA UDI
Seaspine Orthopedics Corporation·10889981158309·Lateral Implant, 18mm x 12mm x 40mm, 10 Deg
Regatta
FDA UDI
Seaspine Orthopedics Corporation·10889981158316·Lateral Implant, 18mm x 12mm x 40mm, 15 Deg
Regatta Lateral System
FDA UDI
Seaspine Orthopedics Corporation·10889981158293·Lateral Implant, 18mm x 12mm x 40mm, 0 Deg
CLOSED FUSION PLATE, MTP PLATE, TALUS PLATE, MODEL 824077021, 22; 824677021, 22, 824071001, 824071101, 824671001, 82467
FDA 510(k)
FDA Class 2
·Orthopedic
TIGER DISCECTOMY DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 19, 2017
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·November 4, 2022
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016
ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 15, 2015
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
SP MAGNET 3
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 13, 2016
COCHLEAR BAHA ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 8, 2025
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE INC·Product code LZG·October 14, 2014
AMPHIRION DEEP PTA BALLOON CATHETER
FDA Adverse Event
Injury
·INVATEC SPA·Product code DQY·June 21, 2013
LEAD MODEL 304
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·July 8, 2011