47 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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S.I.N. Instrument Kits
FDA 510(k)
FDA Class 2
·General Hospital
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693220514·The blades and knifes consumables are for use w...
LEONE SPA
FDA UDI
LEONE SPA·08033707040033·DB BRACKETS MINI 22 BVLD ANT
15mm x 13mm Cervical Rasps
FDA UDI
XENCO MEDICAL LLC·B064XM12220051·15mm x 13mm Cervical Rasps
SYNTHES MIDFACE DISTRACTOR
FDA 510(k)
FDA Class 2
·Dental
MAXLOCK EXTREME SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243033·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243095·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243064·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243088·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243057·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243101·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243040·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024243071·
MULTUM
FDA Adverse Event
Malfunction
·CERNER CORPORATION·Product code LNX·May 17, 2011
PERSONA CEMENTED CRUCIATE RETAINING FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·August 4, 2016
PERSONA STEMMED CEMENTED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·August 4, 2016
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·November 6, 2008
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·August 17, 2011
ALARIS PUMP MODULE ADMINISTRATION SET,
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FPA·July 3, 2013