13 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Intra.Ox 2.0 Handheld Tissue Oximeter
FDA 510(k)
FDA Class 2
·Cardiovascular
CMI MAGNETOCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
PIEZOMED
FDA 510(k)
FDA Class 2
·Dental
GLIDEWELL HT IMPLANT Ø5.0 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 10, 2025
GLIDEWELL HT IMPLANT Ø5.0 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 10, 2025
GLIDEWELL HT IMPLANT Ø5.0 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 21, 2025
GLIDEWELL HT IMPLANT Ø5.0 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 21, 2025
GLIDEWELL HT IMPLANT Ø5.0 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 13, 2025
URISYS 1100
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code KHE·November 3, 2015
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·September 27, 2023
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·November 6, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 2, 2011
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 18, 2013