9 results
·
97ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COMBINED MALAR IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909106552·REVELATION DIAMOND 854-016C - 5 PACK
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756371704·CERVICAL PACK
AT HOME DRUG TESTT, MODEL 9150 T
FDA 510(k)
FDA Unclassified
·Unknown
MAHE PERFECT SPINE- PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 4, 2017
ENDOTAK ENDURANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
KNEEALIGN TIBIAL JIG
FDA Adverse Event
Injury
·ORTHALIGN INC.·Product code OLO·November 22, 2010
LIBERTÉ?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·July 2, 2014