27 results · 27ms · Sources: EU EUDAMED, 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

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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