27 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDRAD 1.5T PELVIC IMAGING SYSTEM INTERFACE DEVICE
FDA 510(k)
FDA Class 2
·Radiology
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00530421·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704284980·CALIPER CASTROVIEJO 40 MILLIMETER GRADUATED 6.5"
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704921086·
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809845198·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE LARGE ...
NA
FDA UDI
ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024312050·
NA
FDA UDI
ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024312043·
V/X ASPHERIC TORIC MULTIFOCAL (POLYMACON) SOFT (HYDROPHILIC) LENSES WITH A CLEAR OR BLUE VISIBILITY TINT
FDA 510(k)
FDA Class 2
·Ophthalmic
DISCOVERY ELBOW
FDA 510(k)
FDA Class 2
·Orthopedic
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
DISC LT DSTL HMRL BDY SET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 13, 2011
SOFTCLIX ® PLUS GT LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·April 11, 2013
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC·Product code LFR·May 30, 2008