434 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIONET BM3PLUS PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780169406·Integra® Miltex® Cassette, Slimline 7, Long, 8"...
Malecot
FDA UDI
COOK INCORPORATED·00827002148277·Percutaneous Malecot Nephrostomy Set
FIBONACCI™ PROXIMAL LATERAL TIBIA PLATE, RIGHT, 8 HOLE
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665035261·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694038829·2.0mm x 8mm Midface Screw
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0840080·Distractor, Screw to Screw
K032008
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007
SURGICAL DYNAMICS SPINAL RETRACTOR
FDA 510(k)
FDA Class 2
·Orthopedic
STS RANGE , MODELS STS20,STS30,STS40
FDA 510(k)
FDA Class 2
·Cardiovascular
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD/HUNTINGTON·Product code MJP·October 24, 2008
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·June 6, 2008
ENDO STICH SHORT INSTRUMENT
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code MFJ·May 8, 2008
DONJOY PAIN BUSTER
FDA Adverse Event
Malfunction
·DONJOY DJO, LLC·Product code MEB·February 8, 2008
EASY AIR
FDA Adverse Event
Death
·PRECISION MEDICAL INC.·Product code BTI·October 7, 2010
ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) PISTOL GRIP 36CM - 15MM ACTIVE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GEI·December 8, 2008
LIGAMAX-5MM ENDO CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code FZP·July 24, 2008
EEA XL 25MM STAPLER WITH 3.5MM STAPLES
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDW·September 8, 2008
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013
TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code HCG·May 9, 2011
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·July 23, 2008