12 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APRO 55 Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
MODULAR FLEXIBLE REAMER HEAD, Ø11.5mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665000900·
LEONE SPA
FDA UDI
LEONE SPA·08033707087472·BALL HEAD ABUTMENT 15°IMP 4,1 GH 5MM
LEONE SPA
FDA UDI
LEONE SPA·08033707087434·BALL HEAD ABUTMENT 15°IMP 4,1 GH 1,5MM
LEONE SPA
FDA UDI
LEONE SPA·08033707087458·BALL HEAD ABUTMENT 15°IMP 4,1 GH 3MM
Denture Base Resin
FDA 510(k)
FDA Class 2
·Dental
MightySat -OTC
FDA 510(k)
FDA Class 2
·Cardiovascular
TRUEMETRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH, INC.·Product code NBW·September 9, 2016
BD CTGCTV2 FOR BD MAX¿ SYSTEM
FDA Adverse Event
Malfunction
·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code LSL·July 17, 2025
SCULPTRA
FDA Adverse Event
Injury
·AVENTIS PHARMA GRUPPO LEPETIT S.R.L.·Product code LMH·August 30, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·November 7, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 18, 2013