27 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GUIDED GROWTH SYSTEM EIGHT-PLATE, QUAD-PLATE (STAINLESS STEEL)
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526159860·PROTECT.ACHI ANKLE SUPPORT GRAY V
ACEMST1
FDA UDI
ACEM SPA·08050705890095·ACEMST1.1 ARTICULATED ARM CEILING
Turbo Wire
FDA UDI
ORMCO CORPORATION·00889989028607·TURBO ARCH LOWER 21 X25 PACK/10
Leva® Anterior Interbody System
FDA UDI
Spine Wave, Inc.·10840642108255·Plate, 34 mm (W) x 13 mm (H)
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306818509·Malleable Retractor 1.5" x 4" w/ Protective Edge
Biliary Drainage Tube
FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170046674·
9616240-2006-00344
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00342
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00330
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
PRISMA SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GALLERY LAMINOPLASTY FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
9616240-2006-00349
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616240-2006-00348
FDA Adverse Event
Malfunction
·Product code FDI·June 20, 2006
*
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
9616240-2006-00346
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
TI MATRIXNEURO SCREW SELF-DRILLING 4MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code JEY·December 21, 2016
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·September 23, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 1, 2011