7 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex FiberTak Suture Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
SILVER FOAM WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
M-VU BREAST DENSITY
FDA 510(k)
FDA Class 2
·Radiology
MICROTARGETING ARRAY INSERTION TUBE W/STYLET
FDA Adverse Event
Malfunction
·FHC, INC.·Product code HAW·November 14, 2008
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY INT'L., LTD.·Product code JDI·August 18, 2011
SM104 MSERIES W5TH WHLOBS3/07
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·July 18, 2013
ACCOLADE DR SL MRI (Model L311)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025