9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AXIAL AND OFFSET CROSSLINK PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
FRS LITE FLUORIDE RELEASING SEALANT
FDA 510(k)
FDA Class 2
·Dental
PATIENT EXAM GLOVES (LATEX) MFG. TIANJIN KANG BAO
FDA 510(k)
FDA Class 1
·General Hospital
UNKNOWN PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·June 11, 2019
VANGUARD CR ILOK FEM-RT 70
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·June 11, 2019
SERIES A PAT STD 34 3 PEG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·June 11, 2019
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·May 19, 2014
CELL-DYN 1800 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·November 10, 2010
STELLARIS 20GA POSTERIOR PACK W AFI & FF
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HQC·December 28, 2012