8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GC FUJI ORTHO
FDA 510(k)
FDA Class 2
·Dental
GENICON DISPOSABLE ELECTROSURGICAL INSTRUMENTATION, MODEL 533-005-910
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DePuy Synthes MAXFRAME Multi-Axial Correction System
FDA 510(k)
FDA Class 2
·Orthopedic
FORCE FX-8C GENERATOR (SHANGHAI)
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·August 3, 2015
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 28, 2014
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·January 14, 2011
INDEFLATOR
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024
INDEFLATOR
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024