8 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PowerDot PD-01M
FDA 510(k)
FDA Class 2
·Physical Medicine
CUFFLINK(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5MM/5.5MM - PEEK ONLY, CUFFLINK SP(TM) KNOTLESS ANCHOR WITH INSERTER, 4.5
FDA 510(k)
FDA Class 2
·Orthopedic
PRONTOSAN WOUND IRRIGATION SOLUTION
FDA 510(k)
FDA Unclassified
·Unknown
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 6, 2025
SELUTE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 22, 2011
THERAKOS CELLEX PHOTOPHERESIS SYSTEM
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·October 10, 2014
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL) NON US
FDA Adverse Event
Malfunction
·COSTA RICA·Product code LTI·September 19, 2008
BIOLOX DELTA LNR 36MM 62-70MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·December 20, 2024