15 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PEREGRINE TAPERED DIFFUSION PROBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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
Analyzer, Medical Image
FDA Pre-Market Approval
FDA Class 2
·LOGICON CARIES DETECTOR
LED.L, LED.M, LED.G, LED.B
FDA 510(k)
FDA Class 2
·Dental
Centurion POCT System
FDA 510(k)
FDA Class 2
·Orthopedic
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
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
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
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 Recall
Terminated
·The Anspach Effort, Inc.·Product code HBE·November 28, 2012