43 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ROSA ONE Brain application
FDA 510(k)
FDA Class 2
·Neurology
ReLine
FDA UDI
Nuvasive, Inc.·00195377047502·RELINE-O Trial, 7mm H Offset Right L-pop
Zavation
FDA UDI
Zavation LLC·00842166131675·Ti3Z CIF 12mmx14mmx11mm -5 deg
Screwdriver
FDA UDI
Treace Medical Concepts, Inc.·00810111226615·Cannulated Screwdriver
OsteoMed
FDA UDI
OSTEOMED LLC·00845694006729·Drill Guide, Compression, Blunt Cannula
ELMED
FDA UDI
ELMED INCORPORATED·00842180107762·FOOTSWITCH, SINGLE, WATER-SEALED, FOR ELMED ESU...
Orfit
FDA UDI
Orfit Industries NV·05420028754139·
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869692755·MOSS VRS Spannschlüssel Approximator HP
MICROSCAN SYNERGIES PLUS
FDA 510(k)
FDA Class 2
·Microbiology
MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AMT RIGHT ANGLE EXTENSION 12"
FDA Adverse Event
Injury
·APPLIED MEDICAL TECHNOLOGY, INC·Product code KNT·December 28, 2020
LIGHTSHEER (ALL MODELS)
FDA Adverse Event
Injury
·*·Product code GEX·March 2, 2006
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWS·February 8, 2014
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·April 10, 2013
DEEP BRAIN STIMULATION DEVICE
FDA Adverse Event
Other
·MEDTRONIC NEUROMODULATION·Product code MHY·September 21, 2007
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008
STOCKERT 70 RF GENERATOR
FDA Adverse Event
Injury
·STOCKERT GMBH·Product code DRF·August 11, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 1, 2013
V.A.C. THERAPY
FDA Adverse Event
Injury
·KCI USA INC.·Product code OMP·February 23, 2015
V.A.C. THERAPY
FDA Adverse Event
Injury
·KCI USA INC.·Product code OMP·February 23, 2015