307 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PICO 7 Single Use Negative Pressure Wound Therapy System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
External Fixation
FDA UDI
Life Spine, Inc.·00190837023706·Inline Hinge
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM
Persona® The Personalized Knee®
FDA UDI
Zimmer, Inc.·00889024238732·
SANTORINI™ Corpectomy Cage System
FDA UDI
VB Spine LLC·10888857243057·Bone Funnel
ALLURA XPER OR TABLE SERIES
FDA 510(k)
FDA Class 2
·Radiology
RK EPIDURAL NEEDLE
FDA 510(k)
FDA Class 2
·Anesthesiology
VITALITY AVT
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·November 9, 2006
HIRES 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS CORP.·Product code MCM·March 6, 2006
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007
MENTOR SMOOTH ROUND MOD
FDA Adverse Event
Other
·MENTOR·Product code FWM·July 21, 2006
VITALITY AVT
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007
CASTLE
FDA Adverse Event
Other
·GETINGE USA·Product code FSY·August 19, 2005
VITALITY AVT
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·November 9, 2006
CASTLE
FDA Adverse Event
Other
·GETINGE USA·Product code FSY·August 19, 2005
VITALITY AVT
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·November 9, 2006
VITALITY AVT FAST-CHARGE
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·May 9, 2006
VITALITY AVT
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007
PROX ACCESS 55MM ART STAP THIC
FDA Adverse Event
ETHICON ENDO-SURGERY, INC.·Product code GAG·October 14, 2005