8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
THE CORIFIX LIGAMENT ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
artegral HD
FDA UDI
Merz Dental GmbH·D7091973005·posteriors; shade A1; size M; lower jaw
Tube Occulsion Clamps
FDA UDI
KOROS U.S.A., INC.·10840199540577·Tube Occulsion Clamps w/ Guard 14cm 5-1/2"
ELITE GLASS
FDA 510(k)
FDA Class 2
·Dental
SURECELL Gelling Fiber Wound Dressing
FDA 510(k)
FDA Unclassified
·Unknown
END CAP T2 TIBIA +5 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·February 21, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 20, 2011
LAPAROSCOPIC TISSUE SEALER
FDA Adverse Event
Injury
·ETHICON-ENDO SURGERY INC.·Product code GEI·July 29, 2014