8 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Suture Wing
FDA 510(k)
FDA Class 2
·Orthopedic
HEARTSTART XL+DEFIBRILLATOR/MONITOR WITH END-TIDAL CARBON DIOXIDE MONITORING
FDA 510(k)
FDA Class 3
·Cardiovascular
VARIAN, INC. ONTRAK TESTCUP AND ONTRAK TESTSTIK
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2025
LANCET DEVICE SNSRTR CMFRT EN
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code MDS·November 6, 2014
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FRN·September 2, 2011
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·July 18, 2013
23-3659-0 PURELL HAND SANITIZER GEL 12FL. OZ. 12/CS
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, LP - READYCARE HARTLAND·Product code LRJ·December 22, 2025