29 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ACUMATCH M-SERIES EXTRA-SMALL METAPHYSEAL SEGMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950018819·FORCEP TISSUE DELICATE 1X2 TEETH 6" 15CM
Waterlase Laser Tips
FDA UDI
Biolase, Inc.·00647529003008·A reusable fiberoptic accessory intended for us...
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040013588·Zirlux 16+ A1 98.5X16
Diverted Bone Tube
FDA UDI
SPINEOLOGY INC.·M7401011081·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226414·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226421·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226384·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226407·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226391·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033226438·
ACUMATCH L-SERIES UNIPOLAR ENDOPROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
BIOZ.PC HEMODYNAMIC MONITOR MODEL BZ-500/BZ-501; BIOZ.PC USER SOFTWARE INSTALLATION KIT MODEL BZ-810
FDA 510(k)
FDA Class 2
·Cardiovascular
LIFEPAK CR2 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·February 21, 2025
BOWEL GRASPER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·April 1, 2014
UNKNOWN MECHANICAL HEART VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWQ·June 24, 2022
QUADRA H CEMENTLESS STEM SIZ 5 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·March 14, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·March 8, 2011
TENDRIL DX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008
UNKNOWN MECHANICAL HEART VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWQ·June 24, 2022