115 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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INTEGRATE -C Interbody Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063494·The blades and knifes consumables are for use w...
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693220507·The blades and knifes consumables are for use w...
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776165970·Freeman Petite Face Lift Retractor W
SANTORINI™ Corpectomy Cage System
FDA UDI
VB Spine LLC·10888857020955·Solid Cage
18M - Five Star Safety
FDA UDI
Certified Safety Manufacturing, Inc.·00766588220048·18M - Five Star Safety
18M - Five Star Safety - w/Logo
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620046·18M - Five Star Safety - w/Logo
MyoSPECT, MyoSpect ES
FDA 510(k)
FDA Class 2
·Radiology
CARDIAC OUTPUT KIT, MODEL CO-1 & INLINE SENSOR CABLE, MODEL ILS-1
FDA 510(k)
FDA Class 2
·Cardiovascular
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242982·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243002·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243026·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242951·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243019·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242975·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242968·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242999·
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code DTB·February 10, 2005
ENDO CLIP II MED/LRG 10MM PISTOL GRIP
FDA Adverse Event
Malfunction
·NORTH HAVEN-USS·Product code FZP·October 21, 2004
SALUTE FIXATION DEVICE
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·October 18, 2004