43 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FiteBac Antimicrobial Cavity Cleanser
FDA 510(k)
FDA Class 2
·Dental
ReLine
FDA UDI
Nuvasive, Inc.·00195377047694·RELINE-O Trial,10mm H Ang Right L-pop
Ceramco® iC
FDA UDI
Dentsply International Inc.·D00142006140·D2
OsteoMed
FDA UDI
OSTEOMED LLC·00845694060424·TAG, STANDARD SCREW, SELF TAP
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68120061400000·Bone Tap Sleeve
IRRIGATING CANNULA
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HALLMARK ANTERIOR CERVCIAL PLATE SYSTEM, HALLMARK FIVE-LEVEL CERVICAL PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
REVISION MODULAR STEM Ø20MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·January 18, 2022
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·October 24, 2014
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011
STERRAD® CYCLESURE® 24 BIOLOGICAL INDICATOR
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code FRC·July 1, 2013
CUSTOM COMBI SET
FDA Adverse Event
Malfunction
·REYNOSA MANUFACTURING·Product code FJK·June 12, 2006
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 27, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 27, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code NRA·July 28, 2015