26 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO XPS 3000 SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
XPS® BUR GUARD - VISAO®
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ERL·April 22, 2016
XPS® BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 13, 2017
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890113210·Zirlux Titanium Blank Abutment compatible with:...
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365106972·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440872·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440919·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440902·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440926·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440889·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033440896·
MODULAR FOOT SYSTEM - 2.7 MM MODULE
FDA 510(k)
FDA Class 2
·Orthopedic
ALL-PRO 2010
FDA 510(k)
FDA Class 2
·Radiology
CONTACT DETACH
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 7, 2025
DR. DON'S ARM CANOE; VELCRO; (20801-V); STERILE
FDA Adverse Event
Malfunction
·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code CCX·February 11, 2022
TEMPBOND CLEAR WITH TRICLOSAN
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EMA·March 19, 2013
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 4, 2011
STARCLOSE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·March 11, 2008
UNKNOWN COMPREHENSIVE REVERSE BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 16, 2023
UNKNOWN COMPREHENSIVE REVERSE TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 16, 2023