459 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex Virtual Implant Positioning (VIP) System
FDA 510(k)
FDA Class 2
·Orthopedic
Altus Spine Interbody Fusion System
FDA UDI
Altus Spine, LLC·00843210131566·Broach Trial
16PW - Class A 21 White Cap - Poly White
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620077·16PW - Class A 21 White Cap - Poly White
Symmetry Maxwell
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482059401·Symmetry® Retractor, Maxwell Flap, 22 mm Wide, ...
17mm x 13.5mm Cervical Rasps
FDA UDI
XENCO MEDICAL LLC·B064XM12220071·17mm x 13.5mm Cervical Rasps
LZI Oxycodone III Enzyme Immunoassay
FDA 510(k)
FDA Class 2
·Clinical Toxicology
LIBERTY 5000 BREAST COIL WITH DISPOSABLE BIOPSY PLATES
FDA 510(k)
FDA Class 2
·Radiology
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243248·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243255·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243231·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243262·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243200·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243194·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243224·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243217·
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962113943·MAXWELL FLAP RETRACTOR, 4", 22MM WIDE
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, LTD. / HUNTINGTON·Product code MFK·June 21, 2007
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC / HUNTINGTON·Product code HQL·June 21, 2007
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC / HUNTINGTON·Product code HQL·June 21, 2007
CAREFREE BODY SHAPE LONG PANTILINERS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON, INC.·Product code HHL·November 1, 2007