354 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127360·2.0 X 6mm Cannulated Headed Screw, T7
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005449·90mm x 90mm Pre-Formed Osteoform Mesh Plate
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005456·90mm x 90mm Preformed Osteoform Mesh, Sterile
CRYOMEGA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AMS SPECTRA CONCEALABLE PENILE PROSTHESIS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818323·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818293·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818347·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818309·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818316·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818330·
SALUTE FIXATION DEVICE
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·April 3, 2006
ENDO GIA II 45-3.5 DLU W/HANDLE (FRANCE)
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GCJ·October 27, 2006
SUPEREAGLE PUNCTUM PLUG
FDA Adverse Event
Injury
·EAGLE VISION, INC.·Product code LZU·February 17, 2006
NEXGEN COMPLETE KNEE SOLUTION LEGACY KNEE-CONSTRAINED CONDYL
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·February 28, 2006
PULMONETIC
FDA Adverse Event
Malfunction
·PULMONETIC SYSTEMS, INC.·Product code CBK·April 17, 2006
SUPEREAGLE PUNCTUM PLUG
FDA Adverse Event
Other
·EAGLE VISION, INC.·Product code LZU·February 17, 2006
SUPEREAGLE PUNCTUM PLUG
FDA Adverse Event
Injury
·EAGLE VISION, INC.·Product code LZU·February 17, 2006
SUPEREAGLE PUNCTUM PLUG
FDA Adverse Event
Other
·EAGLE VISION, INC.·Product code LZU·February 17, 2006