446 results
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22ms
·
Sources: EU EUDAMED, US FDA
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·LOGICON CARIES DETECTOR
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·LOGICON CARIES DETECTOR
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·LOGICON CARIES DETECTOR
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·Logicon Caries Detection Software
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·LOGICON CARIES DETECTOR
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980025·DeltaForm HD lower posteriors, M, A3 -MADE IN G...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756047937·Bias Stockinette 2In X 5Yd1/Pk 20/Cs
PEREGRINE TAPERED DIFFUSION PROBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
ANSPACH***REF 98-0025***Custom MDA Tube for use with MA-D20 Attachment***Rx Only*** This device is intended to be used with Anspach Systems
FDA Enforcement
Class II
·Terminated·The Anspach Effort, Inc.·July 2, 2014
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 7, 2011
CLOSUREFAST CATHETER
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GEI·September 27, 2016
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 24, 2019
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 9, 2016
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
ADAPTA D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015