32 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOVEREIGN
FDA 510(k)
FDA Class 2
·Physical Medicine
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040009994·Zirlux 16+ A2 100X14
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296363·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296370·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296400·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296349·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296387·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296356·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033296394·
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 13, 2026
LORENZ STERNAL CLOSURE SYSTEM WITH MODULAR SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
TORQUE INSTRUMENT, MODEL 8500
FDA 510(k)
FDA Unclassified
·Unknown
PYRAMESH C TITANIUM MESH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code EZX·August 12, 2011
PYRAMESH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code EZX·September 29, 2015
ASTERX EXPANDABLE CORPECTOMY SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019
ASTERX EXPANDABLE CORPECTOMY SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019
PYRAMESH C TITANIUM MESH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code EZX·October 26, 2019
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 27, 2011
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 19, 2013
CE INFUSOR LV 5, 12 PACK
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - IRVINE·Product code MEB·March 9, 2011