7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DTX AND DTX PLUS DISPOSABLE PRESSURE TRANSDUCERS AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
MITEK GIII ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
FHT (FECAL HEME TEST)
FDA 510(k)
FDA Class 2
·Hematology
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·January 30, 2013
ACCELERATOR APS
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JQP·December 22, 2010
PRIMARY TRITANIUM HEMI SOLIDBACK CUP 54MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 15, 2014
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026